A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014719



Internal ID22076350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90935503..90977919hg38UCSC Ensembl
Outerchr4:90931644..90982717hg38UCSC Ensembl
Innerchr4:91856654..91899070hg19UCSC Ensembl
Outerchr4:91852795..91903868hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3851074
hg1951074
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156199
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014719
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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