A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537564



Internal ID18835845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20741749hg38UCSC Ensembl
Innerchr15:20564575..20947078hg19UCSC Ensembl
Innerchr15:18824589..19207088hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38382428
hg19382504
hg18382500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051562
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)nssv3537564
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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