A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568914



Internal ID16009637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32633875..34515668hg38UCSC Ensembl
Innerchr15:32926076..34807869hg19UCSC Ensembl
Innerchr15:30713368..32595161hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381881794
hg191881794
hg181881794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4456n54
Supporting Variantsnssv839792
Samples
Known GenesARHGAP11A, AVEN, CHRM5, EMC4, EMC7, FMN1, GOLGA8A, GREM1, KATNBL1, LOC100131315, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, PGBD4, RYR3, SCG5, SLC12A6, TMCO5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568914
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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