A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007117



Internal ID21916460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124203032..124204001hg38UCSC Ensembl
chr9:126965311..126966280hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38970
hg19970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007117
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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