A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150533



Internal ID19199125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101268262..101271963hg38UCSC Ensembl
Outerchr14:101734599..101738300hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg383702
hg193702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996008
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150533
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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