A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539743



Internal ID20913038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63035125..63045789hg38UCSC Ensembl
chr20:61666477..61677141hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810665
hg1910665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068575
Samples
Known GenesLINC00029, LINC01056, LOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539743
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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