A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081066



Internal ID20648106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180380708..180388862hg38UCSC Ensembl
chr2:181245435..181253589hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg388155
hg198155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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