A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154718



Internal ID15532281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176132836..176384132hg38UCSC Ensembl
Innerchr5:175559839..175811133hg19UCSC Ensembl
Innerchr5:175492445..175743739hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38251297
hg19251295
hg18251295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600341
Supporting Variants
SamplesHGDP01285
Known GenesARL10, KIAA1191, LOC643201, NOP16, SIMC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154718
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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