A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577606



Internal ID16365015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71768203..71772119hg38UCSC Ensembl
Innerchr18:69435439..69439355hg19UCSC Ensembl
Innerchr18:67586419..67590335hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg383917
hg193917
hg183917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6065n54
Supporting Variantsnssv887272, nssv887271, nssv887273
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577606
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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