A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463401



Internal ID21120954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73165667..73174939hg38UCSC Ensembl
chr12:73559447..73568719hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg389273
hg199273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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