A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459349



Internal ID21116902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42152652..42152940hg38UCSC Ensembl
chr12:42546454..42546742hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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