A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781549



Internal ID18815037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:264957..301339hg38UCSC Ensembl
Innerchr3:306640..343022hg19UCSC Ensembl
Innerchr3:281640..318022hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3836383
hg1936383
hg1836383
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893591
Supporting Variants
Samples
Known GenesCHL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781549
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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