A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444132



Internal ID21101685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74273301..74280800hg38UCSC Ensembl
chr9:76888217..76895716hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217802
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444132
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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