A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732604



Internal ID20508528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109769077..109769130hg38UCSC Ensembl
chr9:112531357..112531410hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284565
Samples
Known GenesPALM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732604
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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