A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959032



Internal ID19223213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:84398765..84402165hg38UCSC Ensembl
Outerchr13:84972900..84976300hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg383401
hg193401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118523
Supporting Variants
SamplesKWS1
Known GenesLINC00333
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959032
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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