A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196249



Internal ID22346291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108201934..108202414hg38UCSC Ensembl
chr6:108523138..108523618hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330819
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196249
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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