A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000440



Internal ID20567481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46011181..46011837hg38UCSC Ensembl
chr12:46404964..46405620hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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