A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199549



Internal ID22349117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14684295..14693191hg38UCSC Ensembl
chr6:14684526..14693422hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg388897
hg198897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327519, nssv14327520
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199549
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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