A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140173



Internal ID19260252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:132535800..132535872hg38UCSC Ensembl
Outerchr3:132254644..132254716hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978885
SamplesKWS2
Known GenesDNAJC13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140173
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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