A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146247



Internal ID345452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63150625..63168625hg38UCSC Ensembl
chr20:61781977..61799977hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146247
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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