A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764484



Internal ID16058440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2154875..2158083hg38UCSC Ensembl
Innerchr11:2176105..2179313hg19UCSC Ensembl
Innerchr11:2132681..2135889hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383209
hg193209
hg183209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553071
Supporting Variants
Samples
Known GenesINS-IGF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764484
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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