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dbVar

Database of genomic structural variation

nsv5652151

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

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: 104 SVs from 20 studies. See in: genome view

Submitted genomic57,403,116-57,403,116

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5652151	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	57,403,116	57,403,116
nsv5652151	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	57,437,028	57,437,028

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17084585	insertion	SAMN01096687	Sequencing	Sequence alignment	1,334

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17084585	Submitted genomic		NC_000016.10:g.574 03116_57403117ins1 13	GRCh38 (hg38)		NC_000016.10	Chr16	57,403,116	57,403,116
nssv17084585	Remapped	Perfect	NC_000016.9:g.5743 7028_57437029ins11 3	GRCh37.p13	First Pass	NC_000016.9	Chr16	57,437,028	57,437,028

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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