A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065501



Internal ID18808032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:49001650..49608907hg38UCSC Ensembl
Innerchr22:49397462..50002555hg19UCSC Ensembl
Innerchr22:47783466..48388559hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38607258
hg19605094
hg18605094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4590n100
Supporting Variantsnssv3592333
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065501
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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