A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576642



Internal ID16364051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33521237..33525947hg38UCSC Ensembl
Innerchr18:31101201..31105911hg19UCSC Ensembl
Innerchr18:29355199..29359909hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg384711
hg194711
hg184711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878956, nssv878954, nssv878955
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576642
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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