A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538716



Internal ID18836997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..20838361hg38UCSC Ensembl
Innerchr15:20586733..21043690hg19UCSC Ensembl
Innerchr15:18846747..19308284hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38456882
hg19456958
hg18461538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043174
Supporting Variants
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)nssv3538716
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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