A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441326



Internal ID21098879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109872701..110036200hg38UCSC Ensembl
chr9:112634981..112798480hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38163500
hg19163500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173178
Samples
Known GenesPALM2, PALM2-AKAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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