A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562



Internal ID15551484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:73239788..73284444hg38UCSC Ensembl
Outerchr9:75854704..75899360hg19UCSC Ensembl
Outerchr9:75044524..75089180hg18UCSC Ensembl
Outerchr9:73084258..73128914hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3844657
hg1944657
hg1844657
hg1744657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8610
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)nsv6562
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