A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893541



Internal ID19184361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:209136074..209160213hg38UCSC Ensembl
Outerchr2:209127629..209160214hg38UCSC Ensembl
Innerchr2:210000798..210024937hg19UCSC Ensembl
Outerchr2:209992353..210024938hg19UCSC Ensembl
Innerchr2:209709043..209733182hg18UCSC Ensembl
Outerchr2:209700598..209733183hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3832586
hg1932586
hg1832586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782238, essv25782046, essv25798265, essv25797855, essv25785506
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893541
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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