A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1165



Internal ID15197883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98526305..98560819hg38UCSC Ensembl
Outerchr13:99178559..99213073hg19UCSC Ensembl
Outerchr13:97976560..98011074hg18UCSC Ensembl
Outerchr13:97976560..98011074hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg386482
hg196482
hg186482
hg176482
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142
Supporting Variants
SamplesNA19240
Known GenesSTK24
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)nssv1165
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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