A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564314



Internal ID22433045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142222662..142222662hg38UCSC Ensembl
chr6:142543799..142543799hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330421, nssv14330423, nssv14330422
SamplesNA19238, HG00731, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564314
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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