A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156126



Internal ID22086631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25359694..25365396hg38UCSC Ensembl
Outerchr4:25357757..25372477hg38UCSC Ensembl
Innerchr4:25361316..25367018hg19UCSC Ensembl
Outerchr4:25359379..25374099hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3814721
hg1914721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014118
Samples
Known GenesZCCHC4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156126
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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