A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894086



Internal ID19184940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180900830..181156322hg38UCSC Ensembl
Outerchr4:180892336..181156322hg38UCSC Ensembl
Innerchr4:181821983..182077475hg19UCSC Ensembl
Outerchr4:181813489..182077475hg19UCSC Ensembl
Innerchr4:182058977..182314469hg18UCSC Ensembl
Outerchr4:182050483..182314469hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38263987
hg19263987
hg18263987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800788, essv25779131
Samples
Known GenesLINC00290
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894086
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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