A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025760



Internal ID84909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94334239..94346552hg38UCSC Ensembl
chr9:97096521..97108834hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3812314
hg1912314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141907
Supporting Variants
Samples
Known GenesLOC100132077
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025760
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.026105


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