Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv918186

Organism: Homo sapiens

Study:nstd75 (ClinGen Prenatal)
Variant Type:copy number variation
Method Type:Oligo aCGH
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:284,962

Publication(s):Wapner et al. 2012

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 885 SVs from 68 studies. See in: genome view

Remapped(Score: Perfect):7,163,098-7,448,059

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv918186	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	7,163,098	7,448,059
nsv918186	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	7,213,099	7,498,060
nsv918186	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000016.8	Chr16	7,153,100	7,438,061

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	Copy number
nssv1605275	copy number loss	ISCA_ID_pn_1035	Oligo aCGH	Probe signal intensity	Developmental delay AND/OR other significant developmental or morphological phenotypes	Likely benign	Submitter	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv1605275	Remapped	Perfect	NC_000016.10:g.(?_ 7163098)_(7448059_ ?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	7,163,098	7,448,059
nssv1605275	Remapped	Perfect	NC_000016.9:g.(?_7 213099)_(7498060_? )del	GRCh37.p13	First Pass	NC_000016.9	Chr16	7,213,099	7,498,060
nssv1605275	Submitted genomic		NC_000016.8:g.(?_7 153100)_(7438061_? )del	NCBI36 (hg18)		NC_000016.8	Chr16	7,153,100	7,438,061

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	Sample ID	HGVS	Type	Subject Phenotype	Clinical Interpretation	Source of Interpretation	Gender	Age	Copy number
nssv1605275	ISCA_ID_pn_1035	NCBI36: NC_000016.8:g.(?_7153100)_(7438061_?)del	copy number loss	Developmental delay AND/OR other significant developmental or morphological phenotypes	Likely benign	Submitter	Male	13 weeks gestation	1

No genotype data were submitted for this variant

You are here: NCBI