A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002982



Internal ID20570022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65304151..65313182hg38UCSC Ensembl
chr12:65697931..65706962hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg389032
hg199032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468823
Supporting Variants
Samples
Known GenesMSRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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