A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536526



Internal ID20909873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29478597..29483412hg38UCSC Ensembl
chr21:30850917..30855732hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384816
hg194816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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