A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800641



Internal ID19175011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21968478..22001786hg38UCSC Ensembl
Innerchr1:22294971..22328279hg19UCSC Ensembl
Innerchr1:22167558..22200866hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3833309
hg1933309
hg1833309
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892859
Supporting Variants
Samples
Known GenesCELA3A, CELA3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800641
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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