A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063824



Internal ID19153043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47533888..47555792hg38UCSC Ensembl
Innerchr22:47929637..47951541hg19UCSC Ensembl
Innerchr22:46308301..46330205hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3821905
hg1921905
hg1821905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592273
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)nsv1063824
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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