A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150273



Internal ID15875954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68833759..68923542hg38UCSC Ensembl
Innerchr18:66500996..66590779hg19UCSC Ensembl
Innerchr18:64651976..64741759hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3889784
hg1989784
hg1889784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577370
Supporting Variants
SamplesHGDP00765
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150273
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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