A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576931



Internal ID16364340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52603967..52626592hg38UCSC Ensembl
Innerchr18:50130337..50152962hg19UCSC Ensembl
Innerchr18:48384335..48406960hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3822626
hg1922626
hg1822626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5937n54
Supporting Variantsnssv883296
Samples
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576931
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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