A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527386



Internal ID22396772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106824400..106824456hg38UCSC Ensembl
chr6:107272275..107272331hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330737, nssv14330739, nssv14330738
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527386
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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