A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771048



Internal ID16065004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31940002..31947078hg38UCSC Ensembl
Innerchr11:31961548..31968624hg19UCSC Ensembl
Innerchr11:31918124..31925200hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387077
hg197077
hg187077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553990
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)nssv771048
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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