A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468595



Internal ID21126148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41100848..41124019hg38UCSC Ensembl
chr12:41494650..41517821hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3823172
hg1923172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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