A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382



Internal ID15551286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:126833201..126878304hg38UCSC Ensembl
Outerchr8:127845446..127890549hg19UCSC Ensembl
Outerchr8:127914628..127959731hg18UCSC Ensembl
Outerchr8:127914628..127959731hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3845104
hg1945104
hg1845104
hg1745104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8554
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)nsv6382
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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