A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549453



Internal ID20922614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41305242..41305755hg38UCSC Ensembl
chr21:42677169..42677682hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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