A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065390



Internal ID18807921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23432253..23588601hg38UCSC Ensembl
Innerchr20:23412890..23569238hg19UCSC Ensembl
Innerchr20:23360890..23517238hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38156349
hg19156349
hg18156349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584663, nssv3584661, nssv3584662
Samples
Known GenesCST11, CST13P, CST8, CST9L, CSTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065390
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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