A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525413



Internal ID22394791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:909593..910671hg38UCSC Ensembl
chr6:910021..910943hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381079
hg19923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7703n152
Supporting Variantsnssv14324714, nssv14324711, nssv14324712, nssv14324713, nssv14324715
SamplesHG00512, NA19239, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525413
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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