A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892527



Internal ID19183347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42881405..44112426hg38UCSC Ensembl
Outerchr14:42881405..44112426hg38UCSC Ensembl
Innerchr14:43350608..44581629hg19UCSC Ensembl
Outerchr14:43350608..44581629hg19UCSC Ensembl
Innerchr14:42420358..43651379hg18UCSC Ensembl
Outerchr14:42420358..43651379hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381231022
hg191231022
hg181231022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789679
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892527
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer