A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576932



Internal ID16364341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52603967..52631708hg38UCSC Ensembl
Innerchr18:50130337..50158078hg19UCSC Ensembl
Innerchr18:48384335..48412076hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3827742
hg1927742
hg1827742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5937n54
Supporting Variantsnssv1150595
Samples1780854206_A
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576932
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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