A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112647



Internal ID18904026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:68790783..68795583hg38UCSC Ensembl
Outerchr14:69257500..69262300hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg384801
hg194801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1097n106
Supporting Variantsnssv3967128
SamplesKWS2
Known GenesZFP36L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112647
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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