A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805



Internal ID15544661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62804251..62855271hg38UCSC Ensembl
Outerchr9:66460075..66511095hg19UCSC Ensembl
Outerchr9:66199895..66250915hg18UCSC Ensembl
Outerchr9:64141347..64192367hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3851021
hg1951021
hg1851021
hg1751021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544
Supporting Variants
SamplesNA19240
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)nssv805
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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