A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001854



Internal ID20568894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56513919..56516604hg38UCSC Ensembl
chr12:56907703..56910388hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg382686
hg192686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001854
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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