A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555540



Internal ID20928626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40240515..40244247hg38UCSC Ensembl
chr20:38869155..38872887hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg383733
hg193733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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