A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9920



Internal ID15540005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:34047777..34090442hg38UCSC Ensembl
Outerchr9:34047775..34090440hg19UCSC Ensembl
Outerchr9:34037775..34080440hg18UCSC Ensembl
Outerchr9:34037775..34080440hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3842666
hg1942666
hg1842666
hg1742666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6525
Supporting Variants
SamplesNA18507
Known GenesDCAF12, UBAP2
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)nssv9920
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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