A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10688



Internal ID15195424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133052826..133065502hg38UCSC Ensembl
Outerchr9:135928213..135940889hg19UCSC Ensembl
Outerchr9:134918034..134930710hg18UCSC Ensembl
Outerchr9:132957767..132970443hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3820452
hg1920452
hg1820452
hg1720452
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6746
Supporting Variants
SamplesNA18956
Known GenesCEL, GTF3C5
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)nssv10688
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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