A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441937



Internal ID21099490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128107213..128110600hg38UCSC Ensembl
chr9:130869492..130872879hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383388
hg193388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176856
Samples
Known GenesSLC25A25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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