A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139105



Internal ID19271660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:35667840..35667939hg38UCSC Ensembl
Outerchr3:35709332..35709431hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991727
SamplesKWS2
Known GenesARPP21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139105
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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