A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542599



Internal ID20915857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54149704..54179156hg38UCSC Ensembl
chr20:52766243..52795695hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3829453
hg1929453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067914
Samples
Known GenesCYP24A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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