A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576710



Internal ID16364119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41281660..41288260hg38UCSC Ensembl
Innerchr18:38861624..38868224hg19UCSC Ensembl
Innerchr18:37115622..37122222hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg386601
hg196601
hg186601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv880390
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576710
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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