A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259673



Internal ID20468891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107723536..107723536hg38UCSC Ensembl
chr1:108266158..108266158hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759464
Supporting Variants
Samples
Known GenesVAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259673
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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