A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549295



Internal ID20922463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39660485..39661062hg38UCSC Ensembl
chr20:38289127..38289704hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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