A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555260



Internal ID20928351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25693725..25751366hg38UCSC Ensembl
chr21:27066037..27123677hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3857642
hg1957641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071661
Samples
Known GenesATP5J, GABPA, JAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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