A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529196



Internal ID20902557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1281533..1281949hg38UCSC Ensembl
chr20:1262177..1262593hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066540
Samples
Known GenesSNPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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