A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062436



Internal ID19151655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25296762..25529674hg38UCSC Ensembl
Innerchr22:25692729..25925641hg19UCSC Ensembl
Innerchr22:24022729..24255641hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38232913
hg19232913
hg18232913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4547n100
Supporting Variantsnssv3733437
Samples
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062436
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