A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161516



Internal ID7906230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84900974..85315597hg38UCSC Ensembl
Innerchr7:84530290..84944913hg19UCSC Ensembl
Innerchr7:84368226..84782849hg18UCSC Ensembl
Innerchr7:84174941..84589564hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38414624
hg19414624
hg18414624
hg17414624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422324
Supporting Variants
SamplesND02760
Known GenesSEMA3D
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161516
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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