A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890837



Internal ID19185139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:187162086..187267825hg38UCSC Ensembl
Outerchr1:187162086..187267825hg38UCSC Ensembl
Innerchr1:187131218..187236957hg19UCSC Ensembl
Outerchr1:187131218..187236957hg19UCSC Ensembl
Innerchr1:185397841..185503580hg18UCSC Ensembl
Outerchr1:185397841..185503580hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38105740
hg19105740
hg18105740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796367
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890837
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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