A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114887



Internal ID21298153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71600730..71604278hg38UCSC Ensembl
Innerchr6:72310433..72313981hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383549
hg193549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1042n145
Supporting Variantsnssv14083484
Samplessample14
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114887
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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