A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525531



Internal ID20898892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9079801..9080700hg38UCSC Ensembl
chr20:9060448..9061347hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070818
Samples
Known GenesPLCB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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