A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902021



Internal ID6263948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64655161..64704994hg19UCSC Ensembl
Outerchr14:64647646..64715794hg19UCSC Ensembl
Innerchr14:63724914..63774747hg18UCSC Ensembl
Outerchr14:63717399..63785547hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1560860
SamplesMS24736
Known GenesESR2, SYNE2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902021
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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