A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6128



Internal ID15551006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:26060492..26105282hg38UCSC Ensembl
Outerchr8:25918008..25962798hg19UCSC Ensembl
Outerchr8:25973925..26018715hg18UCSC Ensembl
Outerchr8:25973925..26018715hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3844791
hg1944791
hg1844791
hg1744791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1729
SamplesNA18555
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)nsv6128
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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