A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526178



Internal ID22395558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62349430..62349581hg38UCSC Ensembl
chr1:62815101..62815252hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv244n152
Supporting Variantsnssv14369916, nssv14369915, nssv14369917
SamplesNA19239, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526178
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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