A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199208



Internal ID20766248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107667540..107689885hg38UCSC Ensembl
chr1:108210162..108232507hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3822346
hg1922346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327704
Supporting Variants
Samples
Known GenesVAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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