A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155038



Internal ID22085543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86081695..86105166hg38UCSC Ensembl
Outerchr14:86074249..86118785hg38UCSC Ensembl
Innerchr14:86548039..86571510hg19UCSC Ensembl
Outerchr14:86540593..86585129hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3844537
hg1944537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009706, nssv4009707
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155038
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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