A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476558



Internal ID21134111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118653429..118788326hg38UCSC Ensembl
chr12:119091234..119226131hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38134898
hg19134898
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476558
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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