A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778397



Internal ID19176108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24421934..24446483hg38UCSC Ensembl
Innerchr19:24604736..24629285hg19UCSC Ensembl
Innerchr19:24396576..24421125hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3824550
hg1924550
hg1824550
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893189
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778397
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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