A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154729



Internal ID22085234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21991690..22011632hg38UCSC Ensembl
Outerchr1:21985415..22015896hg38UCSC Ensembl
Innerchr1:22318183..22338125hg19UCSC Ensembl
Outerchr1:22311908..22342389hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3830482
hg1930482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007071, nssv4007070, nssv4007072
Samples
Known GenesCELA3A, CELA3B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154729
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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