A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065776



Internal ID18808307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33464788..33538478hg38UCSC Ensembl
Innerchr22:33860774..33934464hg19UCSC Ensembl
Innerchr22:32190774..32264464hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3873691
hg1973691
hg1873691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4562n100
Supporting Variantsnssv3734203
Samples
Known GenesLARGE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065776
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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