A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738512



Internal ID162178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100136625..100137042hg38UCSC Ensembl
chr9:102898907..102899324hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477305
Supporting Variants
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738512
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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