A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175078



Internal ID15533967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17006008..17299250hg38UCSC Ensembl
Innerchr11:17027555..17320797hg19UCSC Ensembl
Innerchr11:16984131..17277373hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38293243
hg19293243
hg18293243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553568
Supporting Variants
SamplesNINDS_241
Known GenesNUCB2, OR7E14P, PIK3C2A, PLEKHA7, RPS13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175078
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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