A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037902



Internal ID19127121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21760737..21885921hg38UCSC Ensembl
Innerchr14:22229021..22354103hg19UCSC Ensembl
Innerchr14:21298861..21423943hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38125185
hg19125083
hg18125083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712158
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)nsv1037902
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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