A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114970



Internal ID21298236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43776756..43782709hg38UCSC Ensembl
Innerchr19:44280908..44286861hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg385954
hg195954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv579n145
Supporting Variantsnssv14101405
Samplessample322
Known GenesKCNN4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114970
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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