A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893542



Internal ID19184362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208713876..209400284hg38UCSC Ensembl
Outerchr2:208713876..209400284hg38UCSC Ensembl
Innerchr2:209578600..210265008hg19UCSC Ensembl
Outerchr2:209578600..210265008hg19UCSC Ensembl
Innerchr2:209286845..209973253hg18UCSC Ensembl
Outerchr2:209286845..209973253hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38686409
hg19686409
hg18686409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780866
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893542
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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