A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032799



Internal ID89563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44861389..44883078hg38UCSC Ensembl
chr10:45356837..45378526hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3821690
hg1921690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486201
Supporting Variants
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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