A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059705



Internal ID21439002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107723537..107723537hg38UCSC Ensembl
chr1:108266159..108266159hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381870
hg191870
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605761
Supporting Variants
SamplesHG00732
Known GenesVAV3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059705
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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