A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553106



Internal ID20926221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36625427..36634245hg38UCSC Ensembl
chr21:37997725..38006543hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg388819
hg198819
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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