A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101052



Internal ID21278417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36580094..36585700hg38UCSC Ensembl
Innerchr19:37070996..37076602hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385607
hg195607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110198
Supporting Variants
Samplessample27
Known GenesZNF529
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101052
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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