A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160499



Internal ID21508779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134710564..134710626hg38UCSC Ensembl
chr9:137602410..137602472hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589784
Supporting Variants
SamplesNA20847
Known GenesCOL5A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160499
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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