A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046202



Internal ID19135421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62541924..62632010hg38UCSC Ensembl
Innerchr14:63008642..63098728hg19UCSC Ensembl
Innerchr14:62078395..62168481hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3890087
hg1990087
hg1890087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531055
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046202
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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