A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713763



Internal ID19012044
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 StatusS
Merged Variantsnsv1037437
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)nssv3713763
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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