A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891166



Internal ID19185562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101470448..101512040hg38UCSC Ensembl
Outerchr7:101470448..101512040hg38UCSC Ensembl
Innerchr7:101113729..101155321hg19UCSC Ensembl
Outerchr7:101113729..101155321hg19UCSC Ensembl
Innerchr7:100900449..100942041hg18UCSC Ensembl
Outerchr7:100900449..100942041hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3841593
hg1941593
hg1841593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783614
Samples
Known GenesCOL26A1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891166
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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