A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576938



Internal ID16364347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52970314..53062713hg38UCSC Ensembl
Innerchr18:50496684..50589083hg19UCSC Ensembl
Innerchr18:48750682..48843081hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3892400
hg1992400
hg1892400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150597
Samples1780854464_A
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576938
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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