A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713761



Internal ID19012042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..20793234hg38UCSC Ensembl
Innerchr15:20556430..20998563hg19UCSC Ensembl
Innerchr15:18816444..19258613hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38442058
hg19442134
hg18442170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042949
Supporting Variants
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713761
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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