A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532315



Internal ID20905676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32212728..32247006hg38UCSC Ensembl
chr20:30800531..30834809hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3834279
hg1934279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067383
Samples
Known GenesPOFUT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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