A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884982



Internal ID15832252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62102800..62280066hg38UCSC Ensembl
Innerchr18:59770033..59947299hg19UCSC Ensembl
Innerchr18:57921013..58098279hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38177267
hg19177267
hg18177267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577085
Supporting Variants
Samples
Known GenesKIAA1468, PIGN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv884982
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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