A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891210



Internal ID19185606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138679907..138691439hg38UCSC Ensembl
Outerchr7:138679151..138693060hg38UCSC Ensembl
Innerchr7:138364652..138376184hg19UCSC Ensembl
Outerchr7:138363896..138377805hg19UCSC Ensembl
Innerchr7:138015192..138026724hg18UCSC Ensembl
Outerchr7:138014436..138028345hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3813910
hg1913910
hg1813910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800146, essv25797991, essv25781401
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891210
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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