A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535088



Internal ID20908449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25041195..25049461hg38UCSC Ensembl
chr20:25021831..25030097hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg388267
hg198267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067148
Samples
Known GenesACSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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