A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072157



Internal ID20639197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35523919..35529369hg38UCSC Ensembl
chr21:36896217..36901667hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg385451
hg195451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549182
Supporting Variants
Samples
Known GenesLOC100506403
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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