A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022705



Internal ID82822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76367139..76368455hg38UCSC Ensembl
chr9:78982055..78983371hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491149
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022705
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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