A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100613



Internal ID20667653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44694463..44818351hg38UCSC Ensembl
chr3:44735955..44859843hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38123889
hg19123889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362770
Supporting Variants
Samples
Known GenesKIAA1143, KIF15, ZNF501, ZNF502
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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