A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540884



Internal ID20914172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21903506..23807987hg38UCSC Ensembl
chr21:23275826..25180304hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381904482
hg191904479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069961
Samples
Known GenesD21S2088E, LINC00308
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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