A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030924



Internal ID88327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1102042..1102050hg38UCSC Ensembl
chr10:1147982..1147990hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540931
Supporting Variants
Samples
Known GenesWDR37
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030924
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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