A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537636



Internal ID20910972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35245925..35248737hg38UCSC Ensembl
chr21:36618223..36621035hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg382813
hg192813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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