A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038237



Internal ID19127456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20206113..20779072hg38UCSC Ensembl
Innerchr15:20411366..20984401hg19UCSC Ensembl
Innerchr15:18671380..19244450hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38572960
hg19573036
hg18573071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2211n100
Supporting Variantsnssv3538175
Samples
Known GenesCHEK2P2, 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)nsv1038237
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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