A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893753



Internal ID19184573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102574418..102613741hg38UCSC Ensembl
Outerchr3:102574418..102613741hg38UCSC Ensembl
Innerchr3:102293262..102332585hg19UCSC Ensembl
Outerchr3:102293262..102332585hg19UCSC Ensembl
Innerchr3:103775952..103815275hg18UCSC Ensembl
Outerchr3:103775952..103815275hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3839324
hg1939324
hg1839324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784654
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893753
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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