A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528492



Internal ID20901853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11027501..11072700hg38UCSC Ensembl
chr20:11008149..11053348hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3845200
hg1945200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4370n223
Supporting Variantsnssv18066269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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