A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161368



Internal ID7906082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155507387..156354225hg38UCSC Ensembl
Innerchr6:155828521..156675359hg19UCSC Ensembl
Innerchr6:155870213..156717051hg18UCSC Ensembl
Innerchr6:155920634..156767472hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38846839
hg19846839
hg18846839
hg17846839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422505
Supporting Variants
SamplesND03664
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161368
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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