A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3007n106



Internal ID22796835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:190093545..190120945hg38UCSC Ensembl
chr4:191014700..191042100hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3827401
hg1927401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1124905, nsv1132596
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3007n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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