A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636918



Internal ID7023712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74992209..74993113hg38UCSC Ensembl
Innerchr15:74992259..74993063hg38UCSC Ensembl
Outerchr15:74992097..74993225hg38UCSC Ensembl
chr15:75284550..75285454hg19UCSC Ensembl
Innerchr15:75284600..75285404hg19UCSC Ensembl
Outerchr15:75284438..75285566hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15293044
SamplesNA18943
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636918
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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