A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208182



Internal ID22356465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2940583..2940697hg38UCSC Ensembl
chr6:2940817..2940931hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7715n152
Supporting Variantsnssv14324841, nssv14324843, nssv14324839, nssv14324840, nssv14324842
SamplesHG00512, HG00731, HG00732, NA19240, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208182
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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