A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891441



Internal ID19185837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91496676..91534944hg38UCSC Ensembl
Outerchr8:91496676..91534944hg38UCSC Ensembl
Innerchr8:92508904..92547172hg19UCSC Ensembl
Outerchr8:92508904..92547172hg19UCSC Ensembl
Innerchr8:92578080..92616348hg18UCSC Ensembl
Outerchr8:92578080..92616348hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3838269
hg1938269
hg1838269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782266, essv25782346
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891441
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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