A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545607



Internal ID20918833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46366689..46370426hg38UCSC Ensembl
chr20:44995328..44999065hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg383738
hg193738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068384
Samples
Known GenesELMO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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