A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103803



Internal ID20670843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72711984..72718468hg38UCSC Ensembl
chr3:72761135..72767619hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg386485
hg196485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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