A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9385



Internal ID15540336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:162787110..162932892hg38UCSC Ensembl
Outerchr3:162504898..162650680hg19UCSC Ensembl
Outerchr3:163987592..164133374hg18UCSC Ensembl
Outerchr3:163987600..164133382hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38145783
hg19145783
hg18145783
hg17145783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4093
Supporting Variants
SamplesNA18517
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)nssv9385
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