A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455919



Internal ID21113472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66173490..66184364hg38UCSC Ensembl
chr12:66567270..66578144hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3810875
hg1910875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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