A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486791



Internal ID21144344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120269832..120272100hg38UCSC Ensembl
chr12:120707635..120709903hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382269
hg192269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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