A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161477



Internal ID8252880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101974547..102116523hg38UCSC Ensembl
Innerchr9:104736829..104878805hg19UCSC Ensembl
Innerchr9:103776650..103918626hg18UCSC Ensembl
Innerchr9:101816384..101958360hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38141977
hg19141977
hg18141977
hg17141977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422433
Supporting Variants
SamplesND04275
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161477
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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