A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577370



Internal ID16364779
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 StatusM
Merged Variants
Supporting Variantsnssv1150273
SamplesHGDP00765
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577370
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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