A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015237



Internal ID22076868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49449260..49532191hg38UCSC Ensembl
Outerchr1:49443468..49536318hg38UCSC Ensembl
Innerchr1:49914932..49997863hg19UCSC Ensembl
Outerchr1:49909140..50001990hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3892851
hg1992851
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155823
Supporting Variants
Samples
Known GenesAGBL4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015237
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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