A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541359



Internal ID20914641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35485667..35537365hg38UCSC Ensembl
chr21:36857965..36909662hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3851699
hg1951698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072155
Samples
Known GenesLOC100506403
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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