A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022639



Internal ID82780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73975020..73975445hg38UCSC Ensembl
chr9:76589936..76590361hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476532
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000157


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