A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516255



Internal ID20889616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:667241..667802hg38UCSC Ensembl
chr20:647885..648446hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070323
Samples
Known GenesSCRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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