A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040884



Internal ID94972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119305767..119308411hg38UCSC Ensembl
chr10:121065279..121067923hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495396
Supporting Variants
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003434


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