A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4585



Internal ID15192626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36708312..36716232hg38UCSC Ensembl
Outerchr22:37104357..37112277hg19UCSC Ensembl
Outerchr22:35434303..35442223hg18UCSC Ensembl
Outerchr22:35428857..35436777hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg387921
hg197921
hg187921
hg177921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3616
Supporting Variants
SamplesNA12878
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)nssv4585
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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