A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121884



Internal ID18907326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105419763..105420263hg38UCSC Ensembl
Outerchr14:105886100..105886600hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1143n106
Supporting Variantsnssv3968543
SamplesKWS2
Known GenesMTA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121884
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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