A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6677



Internal ID15204924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114214204..114247598hg38UCSC Ensembl
Outerchr9:116976484..117009878hg19UCSC Ensembl
Outerchr9:116016305..116049699hg18UCSC Ensembl
Outerchr9:114056038..114089432hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385890
hg195890
hg185890
hg175890
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5176
SamplesNA19129
Known GenesCOL27A1
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)nsv6677
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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