A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411



Internal ID15551318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:135198368..135243182hg38UCSC Ensembl
Outerchr8:136210611..136255425hg19UCSC Ensembl
Outerchr8:136279793..136324607hg18UCSC Ensembl
Outerchr8:136279793..136324607hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3844815
hg1944815
hg1844815
hg1744815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8563
SamplesNA12156
Known GenesLOC286094
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)nsv6411
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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