A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547161



Internal ID20920367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21752579..21756615hg38UCSC Ensembl
chr21:23124899..23128935hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384037
hg194037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547161
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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