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

dbVar

Database of genomic structural variation

nsv5013489

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:8,135

Publication(s):Abel et al. 2020

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: 277 SVs from 45 studies. See in: genome view

Submitted genomic84,305,753-84,313,952

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5013489	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	84,305,776 (-23, +23)	84,313,910 (-31, +42)
nsv5013489	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	84,339,382 (-23, +23)	84,347,516 (-31, +42)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16573199	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16573199	Submitted genomic		NC_000016.10:g.(84 305753_84305799)_( 84313879_84313952) dup	GRCh38 (hg38)		NC_000016.10	Chr16	84,305,776 (-23, +23)	84,313,910 (-31, +42)
nssv16573199	Remapped	Perfect	NC_000016.9:g.(843 39359_84339405)_(8 4347485_84347558)d up	GRCh37.p13	First Pass	NC_000016.9	Chr16	84,339,382 (-23, +23)	84,347,516 (-31, +42)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16573199	<0.001	11	29246

You are here: NCBI