A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537924



Internal ID18836205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20086048..22041063hg38UCSC Ensembl
Innerchr15:20291301..22329014hg19UCSC Ensembl
Innerchr15:18551315..19830378hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381955016
hg192037714
hg181279064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038675
Supporting Variants
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)nssv3537924
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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