A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892679



Internal ID18836813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42568393..42596849hg38UCSC Ensembl
Outerchr15:42568393..42596849hg38UCSC Ensembl
Innerchr15:42860591..42889047hg19UCSC Ensembl
Outerchr15:42860591..42889047hg19UCSC Ensembl
Innerchr15:40647883..40676339hg18UCSC Ensembl
Outerchr15:40647883..40676339hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3828457
hg1928457
hg1828457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798370
Samples
Known GenesHAUS2, STARD9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892679
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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