A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959070



Internal ID18863610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75255559..75301059hg38UCSC Ensembl
Outerchr15:75547900..75593400hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3845501
hg1945501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118560
Supporting Variants
SamplesKWS1
Known GenesGOLGA6C, GOLGA6D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959070
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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