A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4615



Internal ID15543357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:136145099..136162739hg38UCSC Ensembl
Outerchr8:137157342..137174982hg19UCSC Ensembl
Outerchr8:137226524..137244164hg18UCSC Ensembl
Outerchr8:137226524..137244164hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3817641
hg1917641
hg1817641
hg1717641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6414
Supporting Variants
SamplesNA19129
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)nssv4615
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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