A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153559



Internal ID18850683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:37162398..37302029hg38UCSC Ensembl
Outerchr14:37631603..37771234hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38139632
hg19139632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002214
SamplesKWB1
Known GenesMIPOL1, SLC25A21, SLC25A21-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153559
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer