A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126367



Internal ID18915489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:68790783..68795883hg38UCSC Ensembl
Outerchr14:69257500..69262600hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1097n106
Supporting Variantsnssv3984609
SamplesKWS1
Known GenesZFP36L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126367
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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