A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6126



Internal ID15551004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25538109..25615748hg38UCSC Ensembl
Outerchr8:25395625..25473264hg19UCSC Ensembl
Outerchr8:25451542..25529181hg18UCSC Ensembl
Outerchr8:25451542..25529181hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3877640
hg1977640
hg1877640
hg1777640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5068, nssv8475
SamplesNA12156, NA19129
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)nsv6126
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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