A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101476



Internal ID21284061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15424883..15428992hg38UCSC Ensembl
Innerchr19:15535694..15539803hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg384110
hg194110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118184
Supporting Variants
Samplessample357
Known GenesWIZ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101476
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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