A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10359



Internal ID15195753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:128132278..128140896hg38UCSC Ensembl
Outerchr3:127851121..127859739hg19UCSC Ensembl
Outerchr3:129333811..129342429hg18UCSC Ensembl
Outerchr3:129333819..129342437hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg386869
hg196869
hg186869
hg176869
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3992
Supporting Variants
SamplesNA18956
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv10359
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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