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dbVar

Database of genomic structural variation

nsv5999586

Organism: Homo sapiens

Study:nstd212 (Wu 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:200,083

Publication(s):Wu 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: 600 SVs from 49 studies. See in: genome view

Submitted genomic30,009,341-30,209,423

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5999586	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	30,009,341	30,209,423
nsv5999586	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	30,009,448	30,209,530

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17549765	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17549765	Submitted genomic		NC_000005.10:g.300 09341_30209423dup	GRCh38 (hg38)		NC_000005.10	Chr5	30,009,341	30,209,423
nssv17549765	Remapped	Perfect	NC_000005.9:g.3000 9448_30209530dup	GRCh37.p13	First Pass	NC_000005.9	Chr5	30,009,448	30,209,530

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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