A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515751



Internal ID20889112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5185489..5191917hg38UCSC Ensembl
chr20:5166135..5172563hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg386429
hg196429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068144
Samples
Known GenesCDS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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