A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058681



Internal ID18801212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:567543..606311hg38UCSC Ensembl
Innerchr20:548187..586955hg19UCSC Ensembl
Innerchr20:496187..534955hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838769
hg1938769
hg1838769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589960
Samples
Known GenesTCF15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058681
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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