A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536624



Internal ID20909970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36777901..36785100hg38UCSC Ensembl
chr21:38150202..38157401hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072218
Samples
Known GenesHLCS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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