A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11064



Internal ID15539644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:84896928..84906006hg38UCSC Ensembl
Outerchr3:84946079..84955157hg19UCSC Ensembl
Outerchr3:85028769..85037847hg18UCSC Ensembl
Outerchr3:85028769..85037847hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3815123
hg1915123
hg1815123
hg1715123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3901
Supporting Variants
SamplesNA15510
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)nssv11064
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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