A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139536



Internal ID18934736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131917696..131920496hg38UCSC Ensembl
Outerchr10:133731200..133734000hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977124
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139536
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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