A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426



Internal ID15551334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:140038791..140073817hg38UCSC Ensembl
Outerchr8:141048888..141083915hg19UCSC Ensembl
Outerchr8:141118070..141153097hg18UCSC Ensembl
Outerchr8:141118070..141153097hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3835027
hg1935028
hg1835028
hg1735028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8567
SamplesNA12156
Known GenesTRAPPC9
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)nsv6426
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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