A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552711



Internal ID20925837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16418253..16418870hg38UCSC Ensembl
chr21:17790573..17791190hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070880
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552711
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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