A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173178



Internal ID20740218
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 StatusS
Merged Variantsnsv6441326
Supporting Variants
Samples
Known GenesPALM2, PALM2-AKAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173178
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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