A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442897



Internal ID21100450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122185307..122189620hg38UCSC Ensembl
chr9:124947586..124951899hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg384314
hg194314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176373
Samples
Known GenesMORN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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