A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536906



Internal ID20910250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18046689..18057890hg38UCSC Ensembl
chr21:19419007..19430208hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3811202
hg1911202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069477
Samples
Known GenesCHODL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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