A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546049



Internal ID20919269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48799901..48800321hg38UCSC Ensembl
chr20:47416438..47416858hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068952
Samples
Known GenesPREX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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