A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548890



Internal ID20922068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34100764..34101569hg38UCSC Ensembl
chr21:35473063..35473868hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072005
Samples
Known GenesMRPS6, SLC5A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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