A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537787



Internal ID20911122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:20295710..20844915hg38UCSC Ensembl
chr21:21668022..22217233hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38549206
hg19549212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069594
Samples
Known GenesLINC00320
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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