A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893225



Internal ID19184045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47237234..47289927hg38UCSC Ensembl
Outerchr19:47237234..47289927hg38UCSC Ensembl
Innerchr19:47740491..47793184hg19UCSC Ensembl
Outerchr19:47740491..47793184hg19UCSC Ensembl
Innerchr19:52432331..52485024hg18UCSC Ensembl
Outerchr19:52432331..52485024hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3852694
hg1952694
hg1852694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797354
Samples
Known GenesCCDC9, PRR24
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893225
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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