A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796119



Internal ID19178419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134986279..134993772hg38UCSC Ensembl
Innerchr7:134671030..134678523hg19UCSC Ensembl
Innerchr7:134321570..134329063hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg387494
hg197494
hg187494
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891208
Supporting Variants
Samples
Known GenesAGBL3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796119
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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