A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206578



Internal ID22355097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150322298..150326696hg38UCSC Ensembl
chr6:150643434..150647832hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384399
hg194399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8144n152
Supporting Variantsnssv14331214, nssv14331213
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206578
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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