A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071512



Internal ID20638552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41434481..41435051hg38UCSC Ensembl
chr21:42806408..42806978hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554294
Supporting Variants
Samples
Known GenesMX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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