A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886475



Internal ID16180431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68583998..68653928hg38UCSC Ensembl
Innerchr18:66251235..66321165hg19UCSC Ensembl
Innerchr18:64402215..64472145hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3869931
hg1969931
hg1869931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577367
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)nssv886475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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