A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv767048



Internal ID16061004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8179758..8194306hg38UCSC Ensembl
Innerchr11:8201305..8215853hg19UCSC Ensembl
Innerchr11:8157881..8172429hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3814549
hg1914549
hg1814549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553445
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)nssv767048
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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