A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588318



Internal ID21780361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74086552..74086616hg38UCSC Ensembl
chr9:76701468..76701532hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005884
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588318
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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