A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6307



Internal ID15551203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:93326323..93369361hg38UCSC Ensembl
Outerchr8:94338551..94381589hg19UCSC Ensembl
Outerchr8:94407727..94450765hg18UCSC Ensembl
Outerchr8:94407727..94450765hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3843039
hg1943039
hg1843039
hg1743039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8527
SamplesNA12156
Known GenesLINC00535
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)nsv6307
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer