A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143074



Internal ID18906302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:2299674..2299770hg38UCSC Ensembl
Outerchr4:2301401..2301497hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979841
SamplesKWS2
Known GenesZFYVE28
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143074
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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