A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894110



Internal ID19184964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1023940..1044424hg38UCSC Ensembl
Outerchr5:1023940..1044424hg38UCSC Ensembl
Innerchr5:1024055..1044539hg19UCSC Ensembl
Outerchr5:1024055..1044539hg19UCSC Ensembl
Innerchr5:1077055..1097539hg18UCSC Ensembl
Outerchr5:1077055..1097539hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3820485
hg1920485
hg1820485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779326
Samples
Known GenesNKD2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894110
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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