A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14308907



Internal ID22188871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97781298..97781351hg38UCSC Ensembl
chr3:97500142..97500195hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525660
Supporting Variants
SamplesHG00731
Known GenesARL6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14308907
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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