A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516224



Internal ID20889585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1023201..1024500hg38UCSC Ensembl
chr20:1003844..1005143hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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