A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531998



Internal ID20905359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23740025..23815840hg38UCSC Ensembl
chr20:23720662..23796477hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3875816
hg1975816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066872
Samples
Known GenesCST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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