A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6274



Internal ID15537589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62805316..62855044hg38UCSC Ensembl
Outerchr9:66461140..66510868hg19UCSC Ensembl
Outerchr9:66200960..66250688hg18UCSC Ensembl
Outerchr9:64142412..64192140hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3849729
hg1949729
hg1849729
hg1749729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6544
Supporting Variants
SamplesNA12156
Known GenesPTGER4P2-CDK2AP2P2
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)nssv6274
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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