A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608422



Internal ID21800469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2615276..2697316hg38UCSC Ensembl
chr16:2665277..2747317hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3882041
hg1982041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031306
Supporting Variants
Samples
Known GenesERVK13-1, FLJ42627, KCTD5, LOC652276
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608422
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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