A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893664



Internal ID18837798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14808160..14845522hg38UCSC Ensembl
Outerchr3:14808160..14845522hg38UCSC Ensembl
Innerchr3:14849667..14887029hg19UCSC Ensembl
Outerchr3:14849667..14887029hg19UCSC Ensembl
Innerchr3:14824671..14862033hg18UCSC Ensembl
Outerchr3:14824671..14862033hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3837363
hg1937363
hg1837363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780377
Samples
Known GenesFGD5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893664
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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