A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070880



Internal ID20637920
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 StatusS
Merged Variantsnsv6552711
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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