A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124905



Internal ID19267675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:190093545..190120945hg38UCSC Ensembl
Outerchr4:191014700..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 Variantsdgv3007n106
Supporting Variantsnssv3977711
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124905
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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