A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051249



Internal ID19140468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55457244..55494917hg38UCSC Ensembl
Innerchr14:55923962..55961635hg19UCSC Ensembl
Innerchr14:54993715..55031388hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3837674
hg1937674
hg1837674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531027
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)nsv1051249
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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