A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305358



Internal ID22258633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13682077..13682077hg38UCSC Ensembl
chr3:13723576..13723576hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563223
Supporting Variants
SamplesNA19238
Known GenesLINC00620
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305358
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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