A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608



Internal ID15551534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89144238..89189341hg38UCSC Ensembl
Outerchr9:91759153..91804256hg19UCSC Ensembl
Outerchr9:90948973..90994076hg18UCSC Ensembl
Outerchr9:88988707..89033810hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3845104
hg1945104
hg1845104
hg1745104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8630
SamplesNA12156
Known GenesSHC3
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)nsv6608
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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