A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542865



Internal ID20916116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:24545413..24545868hg38UCSC Ensembl
chr21:25917727..25918182hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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