A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9871



Internal ID15193260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36743578..36765415hg38UCSC Ensembl
Outerchr22:37139623..37161459hg19UCSC Ensembl
Outerchr22:35469569..35491405hg18UCSC Ensembl
Outerchr22:35464123..35485959hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3821838
hg1921837
hg1821837
hg1721837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3617
Supporting Variants
SamplesNA18507
Known GenesIFT27
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)nssv9871
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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