A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438658



Internal ID21096211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69072562..69079807hg38UCSC Ensembl
chr9:71687478..71694723hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg387246
hg197246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185184
Samples
Known GenesFXN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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