A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155021



Internal ID22085526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42395225..42491448hg38UCSC Ensembl
Outerchr14:42392289..42495817hg38UCSC Ensembl
Innerchr14:42864428..42960651hg19UCSC Ensembl
Outerchr14:42861492..42965020hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38103529
hg19103529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv80n97
Supporting Variantsnssv4009451
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155021
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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