A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529381



Internal ID22398773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124877371..124877996hg38UCSC Ensembl
chr10:126565940..126566565hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355907, nssv14355908
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529381
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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