A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6798



Internal ID15551743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:58715885..58749475hg38UCSC Ensembl
Outerchr10:60475645..60509235hg19UCSC Ensembl
Outerchr10:60145651..60179241hg18UCSC Ensembl
Outerchr10:60145651..60179241hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg385848
hg195848
hg185848
hg175848
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8729
SamplesNA12156
Known GenesBICC1, FAM133CP
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)nsv6798
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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