A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524292



Internal ID20897653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23186101..23195700hg38UCSC Ensembl
chr20:23166738..23176337hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4424n223
Supporting Variantsnssv18066844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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