A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534947



Internal ID20908308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1774600..1776807hg38UCSC Ensembl
chr20:1755246..1757453hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382208
hg192208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066663
Samples
Known GenesLOC100289473
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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