A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139535



Internal ID19261458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:123893684..123896884hg38UCSC Ensembl
Outerchr10:125653200..125656400hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977123
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139535
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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