A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892740



Internal ID19183560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98760495..98778517hg38UCSC Ensembl
Outerchr15:98760495..98778517hg38UCSC Ensembl
Innerchr15:99303724..99321746hg19UCSC Ensembl
Outerchr15:99303724..99321746hg19UCSC Ensembl
Innerchr15:97121247..97139269hg18UCSC Ensembl
Outerchr15:97121247..97139269hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3818023
hg1918023
hg1818023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796288
Samples
Known GenesIGF1R
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892740
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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