A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161407



Internal ID8252653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91108790..91289030hg38UCSC Ensembl
Innerchr6:91818508..91998748hg19UCSC Ensembl
Innerchr6:91875229..92055469hg18UCSC Ensembl
Innerchr6:91875229..92055469hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38180241
hg19180241
hg18180241
hg17180241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422475
Supporting Variants
SamplesND00745
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161407
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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