A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694349



Internal ID15431001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104418268..104495298hg38UCSC Ensembl
Innerchr14:104884605..104961635hg19UCSC Ensembl
Innerchr14:103955650..104032680hg18UCSC Ensembl
Innerchr14:103955650..104032680hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3877031
hg1977031
hg1877031
hg1777031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519840
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694349
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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