A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386866



Internal ID22444736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63720118..63720118hg38UCSC Ensembl
chr15:64012317..64012317hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973273
Supporting Variants
Samples
Known GenesHERC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386866
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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