A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787642



Internal ID19171470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39529254..39547488hg38UCSC Ensembl
Innerchr14:39998458..40016692hg19UCSC Ensembl
Innerchr14:39068209..39086443hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3818235
hg1918235
hg1818235
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892502
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787642
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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