A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778655



Internal ID16072611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69053408..69093190hg38UCSC Ensembl
Innerchr11:68820876..68860658hg19UCSC Ensembl
Innerchr11:68577452..68617234hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3839783
hg1939783
hg1839783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555301
Supporting Variants
Samples
Known GenesTPCN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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