A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072179



Internal ID20639219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36083098..36137209hg38UCSC Ensembl
chr21:37455396..37509507hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3854112
hg1954112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547368
Supporting Variants
Samples
Known GenesCBR3, CBR3-AS1, LOC100133286
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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