A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524761



Internal ID15452054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68979322..69027979hg38UCSC Ensembl
Innerchr18:66646559..66695216hg19UCSC Ensembl
Innerchr18:64797539..64846196hg18UCSC Ensembl
Innerchr18:64797539..64846196hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3848658
hg1948658
hg1848658
hg1748658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700752
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524761
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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