A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893591



Internal ID18837725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:264957..301339hg38UCSC Ensembl
Outerchr3:264957..301339hg38UCSC Ensembl
Innerchr3:306640..343022hg19UCSC Ensembl
Outerchr3:306640..343022hg19UCSC Ensembl
Innerchr3:281640..318022hg18UCSC Ensembl
Outerchr3:281640..318022hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3836383
hg1936383
hg1836383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781549
Samples
Known GenesCHL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893591
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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