A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797354



Internal ID19164888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47237234..47289927hg38UCSC Ensembl
Innerchr19:47740491..47793184hg19UCSC Ensembl
Innerchr19:52432331..52485024hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3852694
hg1952694
hg1852694
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893225
Supporting Variants
Samples
Known GenesCCDC9, PRR24
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797354
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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