A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067424



Internal ID18809955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:671381..911795hg38UCSC Ensembl
Innerchr20:652025..892438hg19UCSC Ensembl
Innerchr20:600025..840438hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38240415
hg19240414
hg18240414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3730378
Samples
Known GenesANGPT4, FAM110A, SCRT2, SLC52A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067424
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