A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072170



Internal ID20639210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35720861..35721409hg38UCSC Ensembl
chr21:37093159..37093707hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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