A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539667



Internal ID20912963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39003801..39006200hg38UCSC Ensembl
chr21:40375727..40378126hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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