A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422438



Internal ID8253221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28444245..28640265hg38UCSC Ensembl
Innerchr9:28444243..28640263hg19UCSC Ensembl
Innerchr9:28434243..28630263hg18UCSC Ensembl
Innerchr9:28434243..28630263hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38196021
hg19196021
hg18196021
hg17196021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161482
SamplesND01757
Known GenesLINGO2
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422438
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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