A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057409



Internal ID18799940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36980351..37037405hg38UCSC Ensembl
Innerchr22:37376392..37433445hg19UCSC Ensembl
Innerchr22:35706338..35763391hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3857055
hg1957054
hg1857054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600871
Samples
Known GenesMPST, TEX33, TST
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057409
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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