A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101332



Internal ID21280227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43532849..43534765hg38UCSC Ensembl
Innerchr19:44037001..44038917hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg381917
hg191917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111724
Supporting Variants
Samplessample295
Known GenesZNF575
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101332
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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