A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038003



Internal ID18780534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32247324..32623392hg38UCSC Ensembl
Innerchr15:32539525..32915593hg19UCSC Ensembl
Innerchr15:30326817..30702885hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38376069
hg19376069
hg18376069
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2544n100
Supporting Variantsnssv3547838, nssv3547837
Samples
Known GenesARHGAP11A, GOLGA8K, GOLGA8O, GOLGA8R, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038003
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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