A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156128



Internal ID22086633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25712604..25729254hg38UCSC Ensembl
Outerchr4:25708142..25729379hg38UCSC Ensembl
Innerchr4:25714226..25730876hg19UCSC Ensembl
Outerchr4:25709764..25731001hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3821238
hg1921238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014120, nssv4014121
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156128
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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