A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4587



Internal ID15192628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36775123..36809711hg38UCSC Ensembl
Outerchr22:37171167..37205755hg19UCSC Ensembl
Outerchr22:35501113..35535701hg18UCSC Ensembl
Outerchr22:35495667..35530255hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg385150
hg195150
hg185150
hg175150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3618
Supporting Variants
SamplesNA12878
Known GenesIFT27, PVALB
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)nssv4587
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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