A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023082



Internal ID83099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63284862..63440862hg38UCSC Ensembl
chr9:67239834..67366296hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38156001
hg19126463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142591
Supporting Variants
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023082
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000647


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