A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1181



Internal ID15545744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:109715956..109750792hg38UCSC Ensembl
Outerchr13:110368303..110403139hg19UCSC Ensembl
Outerchr13:109166304..109201140hg18UCSC Ensembl
Outerchr13:109166304..109201140hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg386162
hg196162
hg186162
hg176162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1172
SamplesNA19240
Known GenesLINC00676
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)nsv1181
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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