A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037437



Internal ID19126656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..20868199hg38UCSC Ensembl
Innerchr15:20556430..21073528hg19UCSC Ensembl
Innerchr15:18816444..19338186hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38517023
hg19517099
hg18521743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3713763
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)nsv1037437
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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