A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569



Internal ID15551491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:76127640..76161457hg38UCSC Ensembl
Outerchr9:78742556..78776373hg19UCSC Ensembl
Outerchr9:77932376..77966193hg18UCSC Ensembl
Outerchr9:75972110..76005927hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385460
hg195460
hg185460
hg175460
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5162
SamplesNA19129
Known GenesPCSK5
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)nsv6569
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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