A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073325



Internal ID20640365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44702704..44703474hg38UCSC Ensembl
chr21:46122619..46123389hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536949
Supporting Variants
Samples
Known GenesTSPEAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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