A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068559



Internal ID20635599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62747152..62782596hg38UCSC Ensembl
chr20:61378504..61413948hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3835445
hg1935445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536835
Supporting Variants
Samples
Known GenesLINC00659, NTSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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