A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089



Internal ID15204277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:15538984..15565828hg38UCSC Ensembl
Outerchr8:15396493..15423337hg19UCSC Ensembl
Outerchr8:15440864..15467708hg18UCSC Ensembl
Outerchr8:15440864..15467708hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3826845
hg1926845
hg1826845
hg1726845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6204
SamplesNA12156
Known GenesTUSC3
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)nsv6089
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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