A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528140



Internal ID22397524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2859414..2859563hg38UCSC Ensembl
chr7:2899048..2899197hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8369n152
Supporting Variantsnssv14334487, nssv14334486, nssv14334485
SamplesHG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528140
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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