A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049349



Internal ID19138568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26680642..26925987hg38UCSC Ensembl
Innerchr14:27149848..27395193hg19UCSC Ensembl
Innerchr14:26219688..26465033hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38245346
hg19245346
hg18245346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528548
Samples
Known GenesMIR4307
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049349
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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