A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068330



Internal ID20635370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45288981..45295638hg38UCSC Ensembl
chr20:43917621..43924278hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386658
hg196658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549429
Supporting Variants
Samples
Known GenesMATN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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