A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454768



Internal ID21112321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35425147..35428977hg38UCSC Ensembl
chr9:35425144..35428974hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383831
hg193831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186087
Samples
Known GenesATP8B5P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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