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

dbVar

Database of genomic structural variation

nsv6055985

Organism: Homo sapiens

Study:nstd212 (Wu 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):Wu 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: 151 SVs from 29 studies. See in: genome view

Submitted genomic102,093,582-102,093,582

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6055985	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	102,093,582	102,093,582
nsv6055985	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	102,559,138	102,559,138

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17520641	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17520641	Submitted genomic		NC_000001.11:g.102 093582_102093583in s53	GRCh38 (hg38)		NC_000001.11	Chr1	102,093,582	102,093,582
nssv17520641	Remapped	Perfect	NC_000001.10:g.102 559138_102559139in s53	GRCh37.p13	First Pass	NC_000001.10	Chr1	102,559,138	102,559,138

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.

You are here: NCBI