A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18003619



Internal ID20570659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80035241..80035980hg38UCSC Ensembl
chr12:80429021..80429760hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18003619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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