A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636922



Internal ID7023716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75239326..75253131hg38UCSC Ensembl
Innerchr15:75239326..75253131hg38UCSC Ensembl
Outerchr15:75238826..75253631hg38UCSC Ensembl
chr15:75531667..75545472hg19UCSC Ensembl
Innerchr15:75531667..75545472hg19UCSC Ensembl
Outerchr15:75531167..75545972hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3813806
hg1913806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15293060
SamplesNA20885
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636922
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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