A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3535898



Internal ID18834179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20734174hg38UCSC Ensembl
Innerchr15:20581439..20939503hg19UCSC Ensembl
Innerchr15:18841453..19199516hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38357989
hg19358065
hg18358064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042041
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)nssv3535898
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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