A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3639



Internal ID15201582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:41571809..41602871hg38UCSC Ensembl
Outerchr22:41967813..41998875hg19UCSC Ensembl
Outerchr22:40297759..40328821hg18UCSC Ensembl
Outerchr22:40292313..40323375hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg388374
hg198374
hg188374
hg178374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6986
SamplesNA12156
Known GenesCSDC2, DESI1, PMM1
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)nsv3639
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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