A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636774



Internal ID7023568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66988970..66995052hg38UCSC Ensembl
Innerchr15:66989470..66994552hg38UCSC Ensembl
Outerchr15:66987970..66996052hg38UCSC Ensembl
chr15:67281308..67287390hg19UCSC Ensembl
Innerchr15:67281808..67286890hg19UCSC Ensembl
Outerchr15:67280308..67288390hg19UCSC Ensembl
Cytoband15q22.32
Allele length
AssemblyAllele length
hg386083
hg196083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15274265, essv15274266
SamplesNA19317, NA19347
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636774
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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