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dbVar

Database of genomic structural variation

nsv6038296

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:110,579

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: 351 SVs from 59 studies. See in: genome view

Submitted genomic110,554,819-110,665,397

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6038296	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	110,554,819	110,665,397
nsv6038296	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	110,425,543	110,536,120

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17611539	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17611539	Submitted genomic		NC_000011.10:g.110 554819_110665397du p	GRCh38 (hg38)		NC_000011.10	Chr11	110,554,819	110,665,397
nssv17611539	Remapped	Good	NC_000011.9:g.1104 25543_110536120dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	110,425,543	110,536,120

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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