A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068577



Internal ID20635617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63061122..63061812hg38UCSC Ensembl
chr20:61692474..61693164hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537979
Supporting Variants
Samples
Known GenesLOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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