A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154886



Internal ID22085391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:25636685..25652773hg38UCSC Ensembl
Outerchr13:25635565..25653063hg38UCSC Ensembl
Innerchr13:26210823..26226911hg19UCSC Ensembl
Outerchr13:26209703..26227201hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3817499
hg1917499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010439, nssv4010440, nssv4010460, nssv4010443, nssv4010455, nssv4010448, nssv4010441, nssv4010447, nssv4010458, nssv4010444, nssv4010445, nssv4010450, nssv4010463, nssv4010461, nssv4010456, nssv4010457, nssv4010453, nssv4010438, nssv4010451, nssv4010454, nssv4010452, nssv4010462, nssv4010465, nssv4010446, nssv4010464, nssv4010459, nssv4010442, nssv4010449
Samples
Known GenesATP8A2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154886
Frequency
Sample Size131
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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