A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517862



Internal ID20891223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12054455..12055019hg38UCSC Ensembl
chr20:12035103..12035667hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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