A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536220



Internal ID20909575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8683801..8706300hg38UCSC Ensembl
chr21:9572634..9595133hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3822500
hg1922500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4514n223
Supporting Variantsnssv18204234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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