A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037799



Internal ID19127018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..22014043hg38UCSC Ensembl
Innerchr15:20262224..22301994hg19UCSC Ensembl
Innerchr15:18522238..19803358hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381957073
hg192039771
hg181281121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2192n100
Supporting Variantsnssv3538402
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nsv1037799
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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