A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890997



Internal ID19185393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167163210..167190769hg38UCSC Ensembl
Outerchr6:167163210..167190769hg38UCSC Ensembl
Innerchr6:167576698..167604257hg19UCSC Ensembl
Outerchr6:167576698..167604257hg19UCSC Ensembl
Innerchr6:167496688..167524247hg18UCSC Ensembl
Outerchr6:167496688..167524247hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3827560
hg1927560
hg1827560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780573
Samples
Known GenesTCP10L2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890997
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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