A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422324



Internal ID7906421
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 StatusM
Merged Variants
Supporting Variantsessv5161516
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)esv2422324
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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