A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2372



Internal ID15194080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36744474..36753111hg38UCSC Ensembl
Outerchr22:37140519..37149155hg19UCSC Ensembl
Outerchr22:35470465..35479101hg18UCSC Ensembl
Outerchr22:35465019..35473655hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg388638
hg198637
hg188637
hg178637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3617
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)nssv2372
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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