A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457326



Internal ID21114879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29051601..29074700hg38UCSC Ensembl
chr12:29204534..29227633hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3823100
hg1923100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457326
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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