A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037386



Internal ID92674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68010880..68010881hg38UCSC Ensembl
chr10:69770637..69770638hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382
hg192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559930
Supporting Variants
Samples
Known GenesHERC4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037386
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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