A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256



Internal ID15551147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:73113588..73129566hg38UCSC Ensembl
Outerchr8:74025823..74041801hg19UCSC Ensembl
Outerchr8:74188377..74204355hg18UCSC Ensembl
Outerchr8:74188377..74204355hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3815979
hg1915979
hg1815979
hg1715979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8511
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)nsv6256
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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