A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535620



Internal ID20908978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38741801..38782800hg38UCSC Ensembl
chr21:40113725..40154724hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3841000
hg1941000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4601n223
Supporting Variantsnssv18203952
Samples
Known GenesLINC00114
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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