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dbVar

Database of genomic structural variation

nsv4432105

Organism: Homo sapiens

Study:nstd172 (Deng et al. 2019)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:60,359

Publication(s):Deng et al. 2019

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: 677 SVs from 76 studies. See in: genome view

Remapped(Score: Perfect):41,140,103-41,200,461

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4432105	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	41,140,103	41,200,461
nsv4432105	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000014.8	Chr14	41,609,306	41,669,664

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15752824	deletion	SMI041	Sequencing	Sequence alignment	593

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15752824	Remapped	Perfect	NC_000014.9:g.4114 0103_41200461del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,140,103	41,200,461
nssv15752824	Submitted genomic		NC_000014.8:g.4160 9306_41669664del	GRCh37.p13		NC_000014.8	Chr14	41,609,306	41,669,664

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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