A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045272



Internal ID19134491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..20913755hg38UCSC Ensembl
Innerchr15:20569939..21119084hg19UCSC Ensembl
Innerchr15:18829953..19383709hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38549070
hg19549146
hg18553757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3713801
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)nsv1045272
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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