A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10614



Internal ID15542184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:32796074..32837200hg38UCSC Ensembl
Outerchr8:32653592..32694718hg19UCSC Ensembl
Outerchr8:32773134..32814260hg18UCSC Ensembl
Outerchr8:32773134..32814260hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3841127
hg1941127
hg1841127
hg1741127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6144
Supporting Variants
SamplesNA18956
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)nssv10614
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