A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891208



Internal ID19185604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134986279..134993772hg38UCSC Ensembl
Outerchr7:134986279..134993772hg38UCSC Ensembl
Innerchr7:134671030..134678523hg19UCSC Ensembl
Outerchr7:134671030..134678523hg19UCSC Ensembl
Innerchr7:134321570..134329063hg18UCSC Ensembl
Outerchr7:134321570..134329063hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg387494
hg197494
hg187494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796119
Samples
Known GenesAGBL3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891208
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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