A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10339



Internal ID15195773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:42630117..42661135hg38UCSC Ensembl
Outerchr3:42671609..42702627hg19UCSC Ensembl
Outerchr3:42646613..42677631hg18UCSC Ensembl
Outerchr3:42646613..42677631hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg388490
hg198490
hg188490
hg178490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3781
Supporting Variants
SamplesNA18956
Known GenesNKTR, ZBTB47
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)nssv10339
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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