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dbVar

Database of genomic structural variation

nsv5250990

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:700

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: 148 SVs from 24 studies. See in: genome view

Submitted genomic49,956,401-49,957,100

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5250990	Submitted genomic		GRCh38.p13	Primary Assembly		NC_000010.11	Chr10	49,956,401	49,957,100
nsv5250990	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_004504302.1	Chr10\|NW_0 04504302.1	135,576	136,275

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16815345	copy number variation	Sequencing	Read depth

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16815345	Submitted genomic		GRCh38.p13		NC_000010.11	Chr10	49,956,401	49,957,100
nssv16815345	Remapped	Perfect	GRCh37.p13	First Pass	NW_004504302.1	Chr10\|NW_0 04504302.1	135,576	136,275

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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