A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9885



Internal ID15539962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:152063263..152085669hg38UCSC Ensembl
Outerchr5:151442824..151465230hg19UCSC Ensembl
Outerchr5:151423017..151445423hg18UCSC Ensembl
Outerchr5:151423017..151445423hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3822407
hg1922407
hg1822407
hg1722407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5071
Supporting Variants
SamplesNA18507
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)nssv9885
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