A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006028



Internal ID21915371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97678616..97679863hg38UCSC Ensembl
chr9:100440898..100442145hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591999
Samples
Known GenesXPA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006028
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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