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dbVar

Database of genomic structural variation

nsv5278812

Organism: Homo sapiens

Study:nstd204 (Chen et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:739,600

Publication(s):Chen 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: 5605 SVs from 107 studies. See in: genome view

Submitted genomic21,896,901-22,636,500

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5278812	Submitted genomic		GRCh38.p13	Primary Assembly		NC_000014.9	Chr14	21,896,901	22,636,500
nsv5278812	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	22,365,081	23,105,185

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16822829	copy number variation	Sequencing	Read depth

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16822829	Submitted genomic		GRCh38.p13		NC_000014.9	Chr14	21,896,901	22,636,500
nssv16822829	Remapped	Good	GRCh37.p13	First Pass	NC_000014.8	Chr14	22,365,081	23,105,185

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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