A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002330



Internal ID21911673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81753971..81754065hg38UCSC Ensembl
chr9:84368886..84368980hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586876
Samples
Known GenesLOC101927502
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002330
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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