A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450187



Internal ID21107740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131118088..131119978hg38UCSC Ensembl
chr9:133993475..133995365hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg381891
hg191891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176954
Samples
Known GenesAIF1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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