A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064719



Internal ID19153938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:32632905..32763650hg38UCSC Ensembl
Innerchr22:33028891..33159636hg19UCSC Ensembl
Innerchr22:31358891..31489636hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38130746
hg19130746
hg18130746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600821
Samples
Known GenesSYN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064719
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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