A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445324



Internal ID21102877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132292199..132312927hg38UCSC Ensembl
chr9:135167586..135188314hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3820729
hg1920729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177036
Samples
Known GenesSETX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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