A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780573



Internal ID19169667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167163210..167190769hg38UCSC Ensembl
Innerchr6:167576698..167604257hg19UCSC Ensembl
Innerchr6:167496688..167524247hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3827560
hg1927560
hg1827560
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890997
Supporting Variants
Samples
Known GenesTCP10L2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780573
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