A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458924



Internal ID21116477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:88775392..88960473hg38UCSC Ensembl
chr12:89169169..89354250hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38185082
hg19185082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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