A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564343



Internal ID22433074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:185635..185635hg38UCSC Ensembl
chr6:185635..185635hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324166
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564343
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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