A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047579



Internal ID19136798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..20833279hg38UCSC Ensembl
Innerchr15:20556430..21038608hg19UCSC Ensembl
Innerchr15:18816444..19303160hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38482103
hg19482179
hg18486717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3536350
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047579
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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