A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894069



Internal ID18838237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168759736..168772928hg38UCSC Ensembl
Outerchr4:168759736..168772928hg38UCSC Ensembl
Innerchr4:169680887..169694079hg19UCSC Ensembl
Outerchr4:169680887..169694079hg19UCSC Ensembl
Innerchr4:169917462..169930654hg18UCSC Ensembl
Outerchr4:169917462..169930654hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3813193
hg1913193
hg1813193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782157
Samples
Known GenesPALLD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894069
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