A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160309



Internal ID21451641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128954249..128954418hg38UCSC Ensembl
chr9:131716528..131716697hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591360
Supporting Variants
SamplesHG01596
Known GenesNUP188
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160309
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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