A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577592



Internal ID16365001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71464747..71770519hg38UCSC Ensembl
Innerchr18:69131983..69437755hg19UCSC Ensembl
Innerchr18:67282963..67588735hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38305773
hg19305773
hg18305773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887254
Samples
Known GenesLOC100505776
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577592
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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