A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037393



Internal ID92679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68071114..68071119hg38UCSC Ensembl
chr10:69830871..69830876hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553645
Supporting Variants
Samples
Known GenesHERC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037393
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00281


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