A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038849



Internal ID19128068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65792982..65863201hg38UCSC Ensembl
Innerchr14:66259700..66329919hg19UCSC Ensembl
Innerchr14:65329453..65399672hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3870220
hg1970220
hg1870220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1926n100
Supporting Variantsnssv3531083
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)nsv1038849
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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