A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038019



Internal ID18780550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95735620..95754429hg38UCSC Ensembl
Innerchr14:96201957..96220766hg19UCSC Ensembl
Innerchr14:95271710..95290519hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3818810
hg1918810
hg1818810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3711385
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)nsv1038019
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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