A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458867



Internal ID21116420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62323901..62325600hg38UCSC Ensembl
chr12:62717682..62719381hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002430
Samples
Known GenesUSP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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