A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462522



Internal ID21120075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15006784..15042693hg38UCSC Ensembl
chr12:15159718..15195627hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3835910
hg1935910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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