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dbVar

Database of genomic structural variation

nsv4715888

Organism: Homo sapiens

Study:nstd195 (Mwapagha et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:100,801

Publication(s):Mwapagha 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: 342 SVs from 50 studies. See in: genome view

Remapped(Score: Perfect):103,282,954-103,383,754

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4715888	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	103,282,954	103,383,754
nsv4715888	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	102,923,401	103,024,201

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv16246057	copy number variation	B381	Sequencing	Paired-end mapping	3	5,743

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16246057	Remapped	Perfect	GRCh38.p12	First Pass	NC_000007.14	Chr7	103,282,954	103,383,754
nssv16246057	Submitted genomic		GRCh37 (hg19)		NC_000007.13	Chr7	102,923,401	103,024,201

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.

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