A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072399



Internal ID20639439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39557486..39606392hg38UCSC Ensembl
chr21:40929413..40978319hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3848907
hg1948907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536535
Supporting Variants
Samples
Known GenesC21orf88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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