A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039392



Internal ID18781923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30796262hg38UCSC Ensembl
Innerchr15:30386399..31088465hg19UCSC Ensembl
Innerchr15:28173691..28875757hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38702067
hg19702067
hg18702067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2496n100
Supporting Variantsnssv3546472, nssv3546470, nssv3546469, nssv3546471, nssv3546468
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039392
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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