A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063541



Internal ID19152760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39653719..39720561hg38UCSC Ensembl
Innerchr22:40049724..40116566hg19UCSC Ensembl
Innerchr22:38379670..38446512hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3866843
hg1966843
hg1866843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4574n100
Supporting Variantsnssv3590802
Samples
Known GenesCACNA1I
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063541
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer