A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456297



Internal ID21113850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43736543..43742068hg38UCSC Ensembl
chr12:44130346..44135871hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg385526
hg195526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000629
Samples
Known GenesPUS7L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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