A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517886



Internal ID15445179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:61918459..61930727hg38UCSC Ensembl
Innerchr14:62385177..62397445hg19UCSC Ensembl
Innerchr14:61454930..61467198hg18UCSC Ensembl
Innerchr14:61454930..61467198hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3812269
hg1912269
hg1812269
hg1712269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695294
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517886
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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