A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544297



Internal ID20917536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35882701..35905800hg38UCSC Ensembl
chr21:37254999..37278098hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3823100
hg1923100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4595n223
Supporting Variantsnssv18203933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544297
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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