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dbVar

Database of genomic structural variation

nsv5200265

Organism: Homo sapiens

Study:nstd205 (Kwong et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:13,408

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: 187 SVs from 41 studies. See in: genome view

Remapped(Score: Perfect):23,594,016-23,607,423

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5200265	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	23,594,016	23,607,423
nsv5200265	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000016.9	Chr16	23,605,337	23,618,744

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis
nssv16736561	duplication	1	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16736561	Remapped	Perfect	NC_000016.10:g.235 94016_23607423dup	GRCh38.p12	First Pass	NC_000016.10	Chr16	23,594,016	23,607,423
nssv16736561	Submitted genomic		NC_000016.9:g.2360 5337_23618744dup	GRCh37.p13		NC_000016.9	Chr16	23,605,337	23,618,744

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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