A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530979



Internal ID20904340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6894401..6902900hg38UCSC Ensembl
chr20:6875048..6883547hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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