A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015392



Internal ID22077023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105788935..105795937hg38UCSC Ensembl
Outerchr4:105782376..105796640hg38UCSC Ensembl
Innerchr4:106710092..106717094hg19UCSC Ensembl
Outerchr4:106703533..106717797hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3814265
hg1914265
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156207
Supporting Variants
Samples
Known GenesGSTCD
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015392
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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