A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121872



Internal ID18911606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:28766394..28767894hg38UCSC Ensembl
Outerchr14:29235600..29237100hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1059n106
Supporting Variantsnssv3968530
SamplesKWS2
Known GenesFOXG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121872
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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