A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6216



Internal ID15551103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:60083177..60098310hg38UCSC Ensembl
Outerchr8:60995736..61010869hg19UCSC Ensembl
Outerchr8:61158290..61173423hg18UCSC Ensembl
Outerchr8:61158290..61173423hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3815134
hg1915134
hg1815134
hg1715134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv734
SamplesNA19240
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)nsv6216
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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