A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099676



Internal ID21269365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56085427..56091320hg38UCSC Ensembl
Innerchr19:56596793..56602689hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385894
hg195897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116335
Supporting Variants
Samplessample138
Known GenesZNF787
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099676
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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