A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6963



Internal ID15536900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:17276845..17299486hg38UCSC Ensembl
Outerchr22:17757735..17780376hg19UCSC Ensembl
Outerchr22:16137735..16160376hg18UCSC Ensembl
Outerchr22:16132289..16154930hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3822642
hg1922642
hg1822642
hg1722642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3552
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)nssv6963
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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