A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662321



Internal ID15398973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68863126..68895658hg38UCSC Ensembl
Innerchr18:66530363..66562895hg19UCSC Ensembl
Innerchr18:64681343..64713875hg18UCSC Ensembl
Innerchr18:64681343..64713875hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3832533
hg1932533
hg1832533
hg1732533
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520275
Supporting Variants
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662321
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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