A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037076



Internal ID92473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74916100..74919796hg38UCSC Ensembl
chr10:76675858..76679554hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383697
hg193697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480263
Supporting Variants
Samples
Known GenesKAT6B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037076
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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