A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194282



Internal ID22344615
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6221n152
Supporting Variantsnssv14309141, nssv14309142, nssv14309140
SamplesHG00731, HG00732, HG00733
Known GenesIL12A-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194282
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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