A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890969



Internal ID19185365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156958723..156991616hg38UCSC Ensembl
Outerchr6:156958723..156991616hg38UCSC Ensembl
Innerchr6:157279857..157312750hg19UCSC Ensembl
Outerchr6:157279857..157312750hg19UCSC Ensembl
Innerchr6:157321549..157354442hg18UCSC Ensembl
Outerchr6:157321549..157354442hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3832894
hg1932894
hg1832894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787055
Samples
Known GenesARID1B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890969
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