A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134897



Internal ID21503082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181984928..181984928hg38UCSC Ensembl
chr3:181702716..181702716hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611098
Supporting Variants
SamplesNA19239
Known GenesLOC100996490
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134897
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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