A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564585



Internal ID22433315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3627014..3627014hg38UCSC Ensembl
chr6:3627248..3627248hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325915, nssv14325913, nssv14325914, nssv14325916, nssv14325912, nssv14325911
SamplesNA19238, NA19239, HG00731, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564585
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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