A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101325



Internal ID21280215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9162842..9179607hg38UCSC Ensembl
Innerchr19:9273518..9290283hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3816766
hg1916766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117261
Supporting Variants
Samplessample295
Known GenesZNF317
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101325
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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