A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176218



Internal ID15853802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479021..134851577hg38UCSC Ensembl
Innerchr11:134348915..134721471hg19UCSC Ensembl
Innerchr11:133854125..134226681hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38372557
hg19372557
hg18372557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556629
Supporting Variants
Samples1780854445_A
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176218
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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