A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465052



Internal ID21122605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14865012..14869194hg38UCSC Ensembl
chr12:15017946..15022128hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg384183
hg194183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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