A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6279



Internal ID15190899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69115850..69138261hg38UCSC Ensembl
Outerchr9:71730766..71753177hg19UCSC Ensembl
Outerchr9:70920586..70942997hg18UCSC Ensembl
Outerchr9:68960320..68982731hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3822412
hg1922412
hg1822412
hg1722412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550
Supporting Variants
SamplesNA12156
Known GenesTJP2
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)nssv6279
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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