A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998754



Internal ID20565794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12285205..12298525hg38UCSC Ensembl
chr12:12438139..12451459hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3813321
hg1913321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458061
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998754
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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