A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886383



Internal ID15833653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67439167..67512592hg38UCSC Ensembl
Innerchr18:65106404..65179829hg19UCSC Ensembl
Innerchr18:63257384..63330809hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3873426
hg1973426
hg1873426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577311
Supporting Variants
Samples
Known GenesDSEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv886383
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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