A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195128



Internal ID20762168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61919875..62253423hg38UCSC Ensembl
chr15:62212074..62545622hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38333549
hg19333549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498207
Supporting Variants
Samples
Known GenesC2CD4A, C2CD4B, VPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00066


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