A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141587



Internal ID19255019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:29320683..29328783hg38UCSC Ensembl
Outerchr8:29178200..29186300hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg388101
hg198101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3800n106
Supporting Variantsnssv3993094
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141587
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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