A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497



Internal ID15551412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:20040401..20085275hg38UCSC Ensembl
Outerchr9:20040399..20085273hg19UCSC Ensembl
Outerchr9:20030399..20075273hg18UCSC Ensembl
Outerchr9:20030399..20075273hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3844875
hg1944875
hg1844875
hg1744875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8591
SamplesNA12156
Known Genes
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)nsv6497
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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