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

dbVar

Database of genomic structural variation

nsv6678900

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,790,338

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: 4839 SVs from 94 studies. See in: genome view

Submitted genomic168,515,191-170,305,528

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6678900	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	168,515,191	170,305,528
nsv6678900	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	169,371,701	171,162,038

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18443322	deletion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18443322	Submitted genomic		NC_000002.12:g.168 515191_170305528de l	GRCh38 (hg38)		NC_000002.12	Chr2	168,515,191	170,305,528
nssv18443322	Remapped	Perfect	NC_000002.11:g.169 371701_171162038de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	169,371,701	171,162,038

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18443322	4e-06	1	276116

You are here: NCBI