A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9745



Internal ID15539856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25105417..25135803hg38UCSC Ensembl
Outerchr8:24962932..24993318hg19UCSC Ensembl
Outerchr8:25018849..25049235hg18UCSC Ensembl
Outerchr8:25018849..25049235hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3830387
hg1930387
hg1830387
hg1730387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6123
Supporting Variants
SamplesNA18507
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)nssv9745
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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