A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891112



Internal ID19185508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54059004..54110080hg38UCSC Ensembl
Outerchr7:54055558..54116368hg38UCSC Ensembl
Innerchr7:54126697..54177773hg19UCSC Ensembl
Outerchr7:54123251..54184061hg19UCSC Ensembl
Innerchr7:54094191..54145267hg18UCSC Ensembl
Outerchr7:54090745..54151555hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3860811
hg1960811
hg1860811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791011, essv25787855
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891112
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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