A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18004358



Internal ID20571398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:88767833..88768231hg38UCSC Ensembl
chr12:89161610..89162008hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18004358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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