A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892859



Internal ID19183679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21977209..22001786hg38UCSC Ensembl
Outerchr1:21966563..22001786hg38UCSC Ensembl
Innerchr1:22303702..22328279hg19UCSC Ensembl
Outerchr1:22293056..22328279hg19UCSC Ensembl
Innerchr1:22176289..22200866hg18UCSC Ensembl
Outerchr1:22165643..22200866hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3835224
hg1935224
hg1835224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786265, essv25781066, essv25800641, essv25786412
Samples
Known GenesCELA3A, CELA3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892859
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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