A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591



Internal ID15204830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:83843879..83878395hg38UCSC Ensembl
Outerchr9:86458794..86493310hg19UCSC Ensembl
Outerchr9:85648614..85683130hg18UCSC Ensembl
Outerchr9:83688348..83722864hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg385509
hg195509
hg185509
hg175509
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2813
SamplesNA18555
Known GenesKIF27
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)nsv6591
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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