A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv726



Internal ID15545373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:32821593..32835137hg38UCSC Ensembl
Outerchr8:32679111..32692655hg19UCSC Ensembl
Outerchr8:32798653..32812197hg18UCSC Ensembl
Outerchr8:32798653..32812197hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3813545
hg1913545
hg1813545
hg1713545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144
Supporting Variants
SamplesNA19240
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)nssv726
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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