A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9869



Internal ID15539942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35346451..35360035hg38UCSC Ensembl
Outerchr22:35742444..35756028hg19UCSC Ensembl
Outerchr22:34072444..34086028hg18UCSC Ensembl
Outerchr22:34066998..34080582hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3814548
hg1914548
hg1814548
hg1714548
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3610
Supporting Variants
SamplesNA18507
Known GenesTOM1
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)nssv9869
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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