A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051931



Internal ID19141150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39661121..39695065hg38UCSC Ensembl
Innerchr14:40130325..40164269hg19UCSC Ensembl
Innerchr14:39200076..39234020hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3833945
hg1933945
hg1833945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530128
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)nsv1051931
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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