A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537700



Internal ID20911035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18786221..18793791hg38UCSC Ensembl
chr21:20158539..20166109hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg387571
hg197571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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