A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796645



Internal ID19178253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850846..40873243hg38UCSC Ensembl
Innerchr19:41356751..41379148hg19UCSC Ensembl
Innerchr19:46048591..46070988hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3822398
hg1922398
hg1822398
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893202
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796645
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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