A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101024



Internal ID21270367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57635140..57640632hg38UCSC Ensembl
Innerchr19:58146508..58152000hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385493
hg195493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114780
Supporting Variants
Samplessample15
Known GenesZNF211
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101024
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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