A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893690



Internal ID19184510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72510194..72527172hg38UCSC Ensembl
Outerchr1:72510194..72527172hg38UCSC Ensembl
Innerchr1:72975877..72992855hg19UCSC Ensembl
Outerchr1:72975877..72992855hg19UCSC Ensembl
Innerchr1:72748465..72765443hg18UCSC Ensembl
Outerchr1:72748465..72765443hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3816979
hg1916979
hg1816979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797357, essv25796909
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893690
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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