A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110977



Internal ID21294243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143835616..143838786hg38UCSC Ensembl
Innerchr2:144593185..144596355hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383171
hg193171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv651n145
Supporting Variantsnssv14106899, nssv14102380
Samplessample37, sample395
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110977
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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