A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8267



Internal ID15188911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:80005634..80042023hg38UCSC Ensembl
Outerchr6:80715351..80751740hg19UCSC Ensembl
Outerchr6:80772070..80808459hg18UCSC Ensembl
Outerchr6:80772070..80808459hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3836390
hg1936390
hg1836390
hg1736390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5370
Supporting Variants
SamplesNA12156
Known GenesTTK
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)nssv8267
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