A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469609



Internal ID21127162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94479602..94500150hg38UCSC Ensembl
chr12:94873378..94893926hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3820549
hg1920549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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