A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469116



Internal ID21126669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80763611..80764254hg38UCSC Ensembl
chr12:81157390..81158033hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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