A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8593



Internal ID15188585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:21634402..21663727hg38UCSC Ensembl
Outerchr9:21634401..21663726hg19UCSC Ensembl
Outerchr9:21624401..21653726hg18UCSC Ensembl
Outerchr9:21624401..21653726hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3829326
hg1929326
hg1829326
hg1729326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500
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)nssv8593
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