A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9463



Internal ID15540414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:72874451..72894314hg38UCSC Ensembl
Outerchr8:73786686..73806549hg19UCSC Ensembl
Outerchr8:73949240..73969103hg18UCSC Ensembl
Outerchr8:73949240..73969103hg17UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3819864
hg1919864
hg1819864
hg1719864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6255
Supporting Variants
SamplesNA18517
Known GenesKCNB2
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)nssv9463
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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