A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035721



Internal ID19124940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20942515hg38UCSC Ensembl
Innerchr15:20581439..21147844hg19UCSC Ensembl
Innerchr15:18841453..19412503hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38566330
hg19566406
hg18571051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3535900
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035721
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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