A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468113



Internal ID21125666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12058591..12063789hg38UCSC Ensembl
chr12:12211525..12216723hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg385199
hg195199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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