A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797357



Internal ID19166066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72510194..72527172hg38UCSC Ensembl
Innerchr1:72975877..72992855hg19UCSC Ensembl
Innerchr1:72748465..72765443hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3816979
hg1916979
hg1816979
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893690
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797357
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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