A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525874



Internal ID15106481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103471035..103484031hg38UCSC Ensembl
Innerchr14:103937372..103950368hg19UCSC Ensembl
Innerchr14:103007125..103020121hg18UCSC Ensembl
Innerchr14:103007125..103020121hg17UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3812997
hg1912997
hg1812997
hg1712997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702074
Samples
Known GenesMARK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525874
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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