A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6662



Internal ID15551594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:110246802..110282183hg38UCSC Ensembl
Outerchr9:113009082..113044463hg19UCSC Ensembl
Outerchr9:112048903..112084284hg18UCSC Ensembl
Outerchr9:110088637..110124018hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3835382
hg1935382
hg1835382
hg1735382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1796, nssv10678, nssv6292
SamplesNA12156, NA18956, NA18555
Known GenesTXN
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)nsv6662
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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