A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539129



Internal ID20912436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36956635..36957834hg38UCSC Ensembl
chr21:38328935..38330134hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072222
Samples
Known GenesHLCS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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