A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9611



Internal ID15193017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35363383..35385153hg38UCSC Ensembl
Outerchr22:35759376..35781146hg19UCSC Ensembl
Outerchr22:34089376..34111146hg18UCSC Ensembl
Outerchr22:34083930..34105700hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3812917
hg1912917
hg1812917
hg1712917
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3611
Supporting Variants
SamplesNA18507
Known GenesHMOX1
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)nssv9611
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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