A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037384



Internal ID92672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68002931..68003159hg38UCSC Ensembl
chr10:69762688..69762916hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491594
Supporting Variants
Samples
Known GenesHERC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037384
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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