A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067670



Internal ID20634711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50593273..50594063hg38UCSC Ensembl
chr20:49209810..49210600hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547792
Supporting Variants
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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