A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101405



Internal ID21282200
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 StatusS
Merged Variantsnsv3114970
Supporting Variants
Samplessample322
Known GenesKCNN4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101405
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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