A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115729



Internal ID21298995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57811316..58011612hg38UCSC Ensembl
Innerchr10:59571076..59771372hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38200297
hg19200297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089057, nssv14087525
Samplessample76, sample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115729
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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