A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684755



Internal ID15421407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68867575..68903186hg38UCSC Ensembl
Innerchr18:66534812..66570423hg19UCSC Ensembl
Innerchr18:64685792..64721403hg18UCSC Ensembl
Innerchr18:64685792..64721403hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3835612
hg1935612
hg1835612
hg1735612
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)nssv684755
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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