A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17683741



Internal ID107407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32922348..32922638hg38UCSC Ensembl
chr10:33211276..33211566hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477819
Supporting Variants
Samples
Known GenesITGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17683741
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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