A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009419



Internal ID22071050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27997327..28048395hg38UCSC Ensembl
Outerchr14:27977913..28051049hg38UCSC Ensembl
Innerchr14:28466533..28517601hg19UCSC Ensembl
Outerchr14:28447119..28520255hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3873137
hg1973137
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155015
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009419
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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