A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156207



Internal ID22086712
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015392
Samples
Known GenesGSTCD
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156207
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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