A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043099



Internal ID19132318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..22093448hg38UCSC Ensembl
Innerchr15:20284054..22381399hg19UCSC Ensembl
Innerchr15:18544068..19882763hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382014648
hg192097346
hg181338696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2192n100
Supporting Variantsnssv3536624
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, 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)nsv1043099
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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