A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464782



Internal ID21122335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77717802..77737153hg38UCSC Ensembl
chr12:78111582..78130933hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3819352
hg1919352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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