A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839789



Internal ID15787059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32604149..34557061hg38UCSC Ensembl
Innerchr15:32896350..34849262hg19UCSC Ensembl
Innerchr15:30683642..32636554hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381952913
hg191952913
hg181952913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568910
Supporting Variants
Samples
Known GenesARHGAP11A, AVEN, CHRM5, EMC4, EMC7, FMN1, GOLGA8A, GOLGA8B, GOLGA8R, 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)nssv839789
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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