A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038949



Internal ID19128168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81077246..81113552hg38UCSC Ensembl
Innerchr14:81543590..81579896hg19UCSC Ensembl
Innerchr14:80613343..80649649hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3836307
hg1936307
hg1836307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531226
Samples
Known GenesTSHR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038949
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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