A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735024



Internal ID20510964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128954232..128954400hg38UCSC Ensembl
chr9:131716511..131716679hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295033
Samples
Known GenesNUP188
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735024
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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