A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553136



Internal ID20926245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48127046..48517034hg38UCSC Ensembl
chr20:46755789..47133572hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38389989
hg19377784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068972
Samples
Known GenesLINC00494
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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