A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577588



Internal ID16364997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71340586..71439297hg38UCSC Ensembl
Innerchr18:69007822..69106533hg19UCSC Ensembl
Innerchr18:67158802..67257513hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3898712
hg1998712
hg1898712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887251
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577588
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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