A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448707



Internal ID21106260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83252492..83259928hg38UCSC Ensembl
chr9:85867407..85874843hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387437
hg197437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190975
Samples
Known GenesFRMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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