A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356436



Internal ID21013989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20912715..20913547hg38UCSC Ensembl
chr3:20954207..20955039hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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