A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3625



Internal ID15548253
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10324
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)nsv3625
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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