A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902113



Internal ID2204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41526566..41526646hg38UCSC Ensembl
chr1:41992237..41992317hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138122
Supporting Variants
Samples
Known GenesHIVEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902113
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.021413


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