A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377



Internal ID15551280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:125567376..125627009hg38UCSC Ensembl
Outerchr8:126579620..126639253hg19UCSC Ensembl
Outerchr8:126648802..126708435hg18UCSC Ensembl
Outerchr8:126648802..126708435hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3859634
hg1959634
hg1859634
hg1759634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1768, nssv3685, nssv5126, nssv10639, nssv11196, nssv6249, nssv769
SamplesNA12156, NA12878, NA18956, NA15510, NA18555, NA19240, 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)nsv6377
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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