A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890791



Internal ID18838407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:12790188..13033344hg38UCSC Ensembl
Outerchr6:12790188..13033344hg38UCSC Ensembl
Innerchr6:12790420..13033576hg19UCSC Ensembl
Outerchr6:12790420..13033576hg19UCSC Ensembl
Innerchr6:12898406..13141562hg18UCSC Ensembl
Outerchr6:12898406..13141562hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38243157
hg19243157
hg18243157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798044
Samples
Known GenesPHACTR1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890791
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