A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072645



Internal ID20639685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37125684..37128836hg38UCSC Ensembl
chr21:38497984..38501136hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg383153
hg193153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554428
Supporting Variants
Samples
Known GenesTTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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