A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071661



Internal ID20638701
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 StatusS
Merged Variantsnsv6555260
Supporting Variants
Samples
Known GenesATP5J, GABPA, JAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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