A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv772172



Internal ID15719442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44886386..44922049hg38UCSC Ensembl
Innerchr11:44907937..44943600hg19UCSC Ensembl
Innerchr11:44864513..44900176hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3835664
hg1935664
hg1835664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554184
Supporting Variants
Samples
Known GenesTSPAN18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv772172
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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