A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677564



Internal ID15414216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107742077..107752345hg38UCSC Ensembl
Innerchr9:110504358..110514626hg19UCSC Ensembl
Innerchr9:109544179..109554447hg18UCSC Ensembl
Innerchr9:107583913..107594181hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3810269
hg1910269
hg1810269
hg1710269
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520911
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677564
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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