A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064299



Internal ID19153518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53779021..53804073hg38UCSC Ensembl
Innerchr20:52395560..52420612hg19UCSC Ensembl
Innerchr20:51828967..51854019hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3825053
hg1925053
hg1825053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4325n100
Supporting Variantsnssv3586082
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)nsv1064299
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