A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544766



Internal ID20918003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26598113..26602885hg38UCSC Ensembl
chr21:27970432..27975204hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384773
hg194773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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