A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732901



Internal ID20508827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85270861..85270929hg38UCSC Ensembl
chr9:87885776..87885844hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732901
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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