A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963349



Internal ID19219414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186712825..186712895hg38UCSC Ensembl
Outerchr4:187633979..187634049hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111286
Supporting Variants
SamplesKWS1
Known GenesFAT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963349
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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