A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560



Internal ID15551482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:72836864..72882527hg38UCSC Ensembl
Outerchr9:75451780..75497443hg19UCSC Ensembl
Outerchr9:74641600..74687263hg18UCSC Ensembl
Outerchr9:72681334..72726997hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3845664
hg1945664
hg1845664
hg1745664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6282
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)nsv6560
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