A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453802



Internal ID21111355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35118939..35124408hg38UCSC Ensembl
chr9:35118936..35124405hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg385470
hg195470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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