A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2909



Internal ID15541647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:99399042..99414979hg38UCSC Ensembl
Outerchr13:100051296..100067233hg19UCSC Ensembl
Outerchr13:98849297..98865234hg18UCSC Ensembl
Outerchr13:98849297..98865234hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg385626
hg195626
hg185626
hg175626
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145
Supporting Variants
SamplesNA18555
Known GenesMIR548AN
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)nssv2909
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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