A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064026



Internal ID18806557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33371199..33506073hg38UCSC Ensembl
Innerchr22:33767185..33902059hg19UCSC Ensembl
Innerchr22:32097185..32232059hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38134875
hg19134875
hg18134875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600828
Samples
Known GenesLARGE, MIR4764
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064026
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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