A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037942



Internal ID19127161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20899276hg38UCSC Ensembl
Innerchr15:20585976..21104605hg19UCSC Ensembl
Innerchr15:18845990..19369248hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38518554
hg19518630
hg18523259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3537264, nssv3714647
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, 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)nsv1037942
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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