A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577373



Internal ID16364782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68979322..68999665hg38UCSC Ensembl
Innerchr18:66646559..66666902hg19UCSC Ensembl
Innerchr18:64797539..64817882hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3820344
hg1920344
hg1820344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886480
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577373
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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