A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893790



Internal ID19184610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87368576..87379428hg38UCSC Ensembl
Outerchr1:87368576..87379428hg38UCSC Ensembl
Innerchr1:87834259..87845111hg19UCSC Ensembl
Outerchr1:87834259..87845111hg19UCSC Ensembl
Innerchr1:87606847..87617699hg18UCSC Ensembl
Outerchr1:87606847..87617699hg18UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3810853
hg1910853
hg1810853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797134
Samples
Known GenesLOC100505768
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893790
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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