A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422365



Internal ID7906462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111932964..112987872hg38UCSC Ensembl
Innerchr7:111573019..112627927hg19UCSC Ensembl
Innerchr7:111360255..112415163hg18UCSC Ensembl
Innerchr7:111166970..112221878hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381054909
hg191054909
hg181054909
hg171054909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161410
SamplesND01757
Known GenesC7orf60, DOCK4, IFRD1, LSMEM1, TMEM168, ZNF277
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422365
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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