A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8098



Internal ID15535766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:40570698..40615677hg38UCSC Ensembl
Outerchr5:40570800..40615779hg19UCSC Ensembl
Outerchr5:40606557..40651536hg18UCSC Ensembl
Outerchr5:40606557..40651536hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3844980
hg1944980
hg1844980
hg1744980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4807
Supporting Variants
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)nssv8098
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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