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dbVar

Database of genomic structural variation

nsv4737394

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:56

Publication(s):Quan 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: 344 SVs from 58 studies. See in: genome view

Remapped(Score: Perfect):17,132,514-17,132,569

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4737394	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	17,132,514	17,132,569
nsv4737394	Remapped	Perfect	GRCh38.p12	PATCHES	Second Pass	NW_019805500.1	Chr16\|NW_0 19805500.1	133,775	133,830
nsv4737394	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	17,226,371	17,226,426

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16288372	deletion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16288372	Remapped	Perfect	NW_019805500.1:g.1 33775_133830del	GRCh38.p12	Second Pass	NW_019805500.1	Chr16\|NW_0 19805500.1	133,775	133,830
nssv16288372	Remapped	Perfect	NC_000016.10:g.171 32514_17132569del	GRCh38.p12	First Pass	NC_000016.10	Chr16	17,132,514	17,132,569
nssv16288372	Submitted genomic		NC_000016.9:g.1722 6371_17226426del	GRCh37 (hg19)		NC_000016.9	Chr16	17,226,371	17,226,426

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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