A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891503



Internal ID19185899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4141108..4381802hg38UCSC Ensembl
Outerchr2:4141108..4381802hg38UCSC Ensembl
Innerchr2:4188698..4429392hg19UCSC Ensembl
Outerchr2:4188698..4429392hg19UCSC Ensembl
Innerchr2:4166573..4407267hg18UCSC Ensembl
Outerchr2:4166573..4407267hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38240695
hg19240695
hg18240695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787166
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891503
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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