A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902104



Internal ID6264031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77722467..77750057hg19UCSC Ensembl
Outerchr14:77720741..77756321hg19UCSC Ensembl
Innerchr14:76792220..76819810hg18UCSC Ensembl
Outerchr14:76790494..76826074hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1530784
SamplesMS10311
Known GenesMIR1260, NGB, POMT2, TMEM63C
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902104
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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