A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9375



Internal ID15540326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:34633833..34696714hg38UCSC Ensembl
Outerchr22:35029825..35092705hg19UCSC Ensembl
Outerchr22:33359825..33422705hg18UCSC Ensembl
Outerchr22:33354379..33417259hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3862882
hg1962881
hg1862881
hg1762881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3606
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)nssv9375
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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