A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455487



Internal ID21113040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131774236..131779412hg38UCSC Ensembl
chr9:134649623..134654799hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385177
hg195177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455487
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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