A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547571



Internal ID20920772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39178912..39180848hg38UCSC Ensembl
chr21:40550838..40552774hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381937
hg191937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072381
Samples
Known GenesPSMG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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