A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057613



Internal ID19146832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26258719..26324931hg38UCSC Ensembl
Innerchr20:26239355..26305567hg19UCSC Ensembl
Innerchr20:26187355..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3866213
hg1966213
hg1866213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584713
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057613
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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