A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469300



Internal ID21126853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90958590..90963904hg38UCSC Ensembl
chr12:91352367..91357681hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg385315
hg195315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005561
Samples
Known GenesEPYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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