A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537922



Internal ID18836203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20086048..22014043hg38UCSC Ensembl
Innerchr15:20291301..22301994hg19UCSC Ensembl
Innerchr15:18551315..19803358hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381927996
hg192010694
hg181252044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044615
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)nssv3537922
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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