A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8642



Internal ID15535222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98546089..98580529hg38UCSC Ensembl
Outerchr9:101308371..101342811hg19UCSC Ensembl
Outerchr9:100348192..100382632hg18UCSC Ensembl
Outerchr9:98387926..98422366hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3834441
hg1934441
hg1834441
hg1734441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6633
Supporting Variants
SamplesNA12156
Known GenesGABBR2
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)nssv8642
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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