A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457860



Internal ID21115413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51257730..51268828hg38UCSC Ensembl
chr12:51651514..51662612hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3811099
hg1911099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196322
Samples
Known GenesSMAGP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457860
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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