A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524908



Internal ID6018659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64700045..64703593hg19UCSC Ensembl
Innerchr14:63769798..63773346hg18UCSC Ensembl
Innerchr14:63769798..63773346hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv700919
Samples
Known GenesESR2
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv524908
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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