A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160967



Internal ID21493589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137485270..137485383hg38UCSC Ensembl
chr9:140379722..140379835hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586603
Supporting Variants
SamplesNA19238
Known GenesPNPLA7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160967
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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