A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137700



Internal ID15644200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77195973..77375037hg38UCSC Ensembl
Innerchr9:79810889..79989953hg19UCSC Ensembl
Innerchr9:79000709..79179773hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38179065
hg19179065
hg18179065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614728
Supporting Variants
Samples
Known GenesVPS13A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137700
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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