A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7745



Internal ID15536119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36880859..36892653hg38UCSC Ensembl
Outerchr22:37276901..37288695hg19UCSC Ensembl
Outerchr22:35606847..35618641hg18UCSC Ensembl
Outerchr22:35601401..35613195hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3811795
hg1911795
hg1811795
hg1711795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3621
Supporting Variants
SamplesNA12156
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)nssv7745
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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