A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453733



Internal ID21111286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132146579..132156976hg38UCSC Ensembl
chr9:135021966..135032363hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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