A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063655



Internal ID19152874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23416012..23509093hg38UCSC Ensembl
Innerchr20:23396649..23489730hg19UCSC Ensembl
Innerchr20:23344649..23437730hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3893082
hg1993082
hg1893082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737177, nssv3584660
Samples
Known GenesCST11, CST8, CSTL1, NAPB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063655
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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