A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038428



Internal ID19127647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20283071..20738717hg38UCSC Ensembl
Innerchr15:20488324..20944046hg19UCSC Ensembl
Innerchr15:18748338..19204074hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38455647
hg19455723
hg18455737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n100
Supporting Variantsnssv3536033
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)nsv1038428
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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