A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178308



Internal ID20745348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74129701..74132000hg38UCSC Ensembl
chr9:76744617..76746916hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449927
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178308
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00921


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