A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745788



Internal ID20521798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96157611..96157778hg38UCSC Ensembl
chr9:98919893..98920060hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745788
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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