A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10321



Internal ID15542477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:34404537..34420818hg38UCSC Ensembl
Outerchr22:34800527..34816808hg19UCSC Ensembl
Outerchr22:33130527..33146808hg18UCSC Ensembl
Outerchr22:33125081..33141362hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg385955
hg195955
hg185955
hg175955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3605
Supporting Variants
SamplesNA18956
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)nssv10321
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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