A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206367



Internal ID22354919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63418684..63419150hg38UCSC Ensembl
chr6:64128589..64129055hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327675, nssv14327676, nssv14327677, nssv14327678
SamplesHG00731, NA19240, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206367
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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