A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471886



Internal ID21129439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80952901..80953800hg38UCSC Ensembl
chr12:81346680..81347579hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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