A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051191



Internal ID19140410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..20868199hg38UCSC Ensembl
Innerchr15:20586733..21073528hg19UCSC Ensembl
Innerchr15:18846747..19338186hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38486720
hg19486796
hg18491440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3538717
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)nsv1051191
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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