A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213078



Internal ID22360135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110140506..110140976hg38UCSC Ensembl
chr10:111900264..111900734hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353812, nssv14353813
SamplesHG00512, HG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213078
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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