A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403



Internal ID15204623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:133132921..133166728hg38UCSC Ensembl
Outerchr8:134145165..134178972hg19UCSC Ensembl
Outerchr8:134214347..134248154hg18UCSC Ensembl
Outerchr8:134214347..134248154hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg385904
hg195904
hg185904
hg175904
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690
SamplesNA12878
Known GenesTG
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)nsv6403
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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