A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126806



Internal ID21439553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72045431..72045431hg38UCSC Ensembl
chr3:72094582..72094582hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607429
Supporting Variants
SamplesHG00732
Known GenesLINC00877
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126806
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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