A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083768



Internal ID20650808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224270304..224270762hg38UCSC Ensembl
chr2:225135021..225135479hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355242
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00063


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