A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582656



Internal ID16023379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:110038675..110225473hg38UCSC Ensembl
Innerchr2:110796252..110983050hg19UCSC Ensembl
Innerchr2:110153541..110340339hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38186799
hg19186799
hg18186799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6999n54
Supporting Variantsnssv916031, nssv916033, nssv916032
Samples
Known GenesLINC00116, MALL, MIR4267, MIR4436B1, MIR4436B2, NPHP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582656
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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