A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194492



Internal ID22344801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107953778..107953876hg38UCSC Ensembl
chr6:108274982..108275080hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8053n152
Supporting Variantsnssv14330799, nssv14330798, nssv14330797
SamplesHG00512, HG00513, HG00514
Known GenesSEC63
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194492
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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