A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890926



Internal ID19185322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191164659..191181929hg38UCSC Ensembl
Outerchr1:191164659..191181929hg38UCSC Ensembl
Innerchr1:191133789..191151059hg19UCSC Ensembl
Outerchr1:191133789..191151059hg19UCSC Ensembl
Innerchr1:189400412..189417682hg18UCSC Ensembl
Outerchr1:189400412..189417682hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3817271
hg1917271
hg1817271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785970
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890926
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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