A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564655



Internal ID22433385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37728325..37728325hg38UCSC Ensembl
chr6:37696101..37696101hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325645, nssv14325643, nssv14325646, nssv14325644, nssv14325647
SamplesNA19238, NA19239, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564655
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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