A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135738



Internal ID21475276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:93886902..93887217hg38UCSC Ensembl
chr3:93605746..93606061hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578909
Supporting Variants
SamplesHG03371
Known GenesPROS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135738
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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