A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154837



Internal ID22085342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:61808789..61817039hg38UCSC Ensembl
Outerchr12:61804490..61818077hg38UCSC Ensembl
Innerchr12:62202570..62210820hg19UCSC Ensembl
Outerchr12:62198271..62211858hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3813588
hg1913588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009240
Samples
Known GenesFAM19A2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154837
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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