A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7673



Internal ID15536191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:33903102..33948153hg38UCSC Ensembl
Outerchr20:32490908..32535959hg19UCSC Ensembl
Outerchr20:31954569..31999620hg18UCSC Ensembl
Outerchr20:31954569..31999620hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3845052
hg1945052
hg1845052
hg1745052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3356
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)nssv7673
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