A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18076582



Internal ID20643623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104211778..104212433hg38UCSC Ensembl
chr2:104828236..104828891hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349640
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18076582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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