A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10324



Internal ID15542474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38625837..38651326hg38UCSC Ensembl
Outerchr22:39021842..39047331hg19UCSC Ensembl
Outerchr22:37351788..37377277hg18UCSC Ensembl
Outerchr22:37346342..37371831hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg386943
hg196943
hg186943
hg176943
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3625
Supporting Variants
SamplesNA18956
Known GenesFAM227A
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)nssv10324
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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