A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000810



Internal ID20567850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33136101..33154500hg38UCSC Ensembl
chr12:33289035..33307434hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3818400
hg1918400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03091


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