A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064509



Internal ID19153728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38890960..38933588hg38UCSC Ensembl
Innerchr22:39286965..39329593hg19UCSC Ensembl
Innerchr22:37616911..37659539hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3842629
hg1942629
hg1842629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4567n100
Supporting Variantsnssv3600887
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)nsv1064509
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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