A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704199



Internal ID127865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64469627..64480488hg38UCSC Ensembl
chr15:64761826..64772687hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3810862
hg1910862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704199
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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