A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000465



Internal ID20567506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46373801..46375700hg38UCSC Ensembl
chr12:46767584..46769483hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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