A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071988



Internal ID20639028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33691689..33696628hg38UCSC Ensembl
chr21:35063994..35068933hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384940
hg194940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552407
Supporting Variants
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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