A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192687



Internal ID22343234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128614497..128614815hg38UCSC Ensembl
chr6:128935642..128935960hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330867, nssv14330868
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192687
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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