A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437579



Internal ID21095132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74218478..74288379hg38UCSC Ensembl
chr9:76833394..76903295hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3869902
hg1969902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221974
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437579
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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