A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691238



Internal ID15427890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13473830..13478884hg38UCSC Ensembl
Innerchr6:13474062..13479116hg19UCSC Ensembl
Innerchr6:13582041..13587095hg18UCSC Ensembl
Innerchr6:13582041..13587095hg17UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385055
hg195055
hg185055
hg175055
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520921
Supporting Variants
Samples
Known GenesGFOD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691238
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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