A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536718



Internal ID20910061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32790063..32790769hg38UCSC Ensembl
chr21:34162374..34163080hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071946
Samples
Known GenesC21orf49, C21orf62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536718
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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