A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14309141



Internal ID22200235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160071929..160072013hg38UCSC Ensembl
chr3:159789716..159789800hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194282
Supporting Variants
SamplesHG00732
Known GenesIL12A-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14309141
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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