A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8526



Internal ID15535338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:93044653..93075417hg38UCSC Ensembl
Outerchr8:94056881..94087646hg19UCSC Ensembl
Outerchr8:94126057..94156822hg18UCSC Ensembl
Outerchr8:94126057..94156822hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3830765
hg1930766
hg1830766
hg1730766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6305
Supporting Variants
SamplesNA12156
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)nssv8526
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