A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523467



Internal ID20896828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1625984..1631286hg38UCSC Ensembl
chr20:1606630..1611932hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385303
hg195303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067118
Samples
Known GenesSIRPG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523467
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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