A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2392



Internal ID15540744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32055379..32068163hg38UCSC Ensembl
Outerchr3:32096871..32109655hg19UCSC Ensembl
Outerchr3:32071875..32084659hg18UCSC Ensembl
Outerchr3:32071875..32084659hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3812785
hg1912785
hg1812785
hg1712785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3750
Supporting Variants
SamplesNA18555
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)nssv2392
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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