A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887251



Internal ID16181207
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 StatusS
Merged Variantsnsv577588
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887251
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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