A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959026



Internal ID19204974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:51690864..51696264hg38UCSC Ensembl
Outerchr13:52265000..52270400hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118517
Supporting Variants
SamplesKWS1
Known GenesWDFY2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959026
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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