A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467509



Internal ID21125062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:74608001..74629400hg38UCSC Ensembl
chr12:75001781..75023180hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3821400
hg1921400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1610n223
Supporting Variantsnssv18003478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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