A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959604



Internal ID19207347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:3570873..3611573hg38UCSC Ensembl
Outerchr4:3572600..3613300hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3840701
hg1940701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118710
Supporting Variants
SamplesKWS1
Known GenesLINC00955
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959604
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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