A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110688



Internal ID21293954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23033891..23037519hg38UCSC Ensembl
Innerchr16:23045212..23048840hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg383629
hg193629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096475, nssv14097861, nssv14099143, nssv14097925, nssv14096338, nssv14096431
Samplessample282, sample232, sample153, sample417, sample304, sample385
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110688
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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