A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800146



Internal ID19173213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138679907..138693060hg38UCSC Ensembl
Innerchr7:138364652..138377805hg19UCSC Ensembl
Innerchr7:138015192..138028345hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3813154
hg1913154
hg1813154
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891210
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800146
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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