A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992772



Internal ID18882132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75258559..75293359hg38UCSC Ensembl
Outerchr15:75550900..75585700hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3834801
hg1934801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141267
Supporting Variants
SamplesKWS2
Known GenesGOLGA6C, GOLGA6D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992772
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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