A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18004172



Internal ID20571212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77390071..77390429hg38UCSC Ensembl
chr12:77783851..77784209hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18004172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00107


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