A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577647



Internal ID16365056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73346075..73441418hg38UCSC Ensembl
Innerchr18:71013310..71108653hg19UCSC Ensembl
Innerchr18:69164290..69259633hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3895344
hg1995344
hg1895344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887373
Samples
Known GenesLOC100505817
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577647
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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