A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18003680



Internal ID20570720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80778702..80779238hg38UCSC Ensembl
chr12:81172481..81173017hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18003680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00108


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