A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544303



Internal ID20917542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8680901..8696700hg38UCSC Ensembl
chr21:9569734..9585533hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3815800
hg1915800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544303
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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