A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636909



Internal ID6677016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74791220..74794723hg38UCSC Ensembl
Innerchr15:74791241..74794702hg38UCSC Ensembl
Outerchr15:74791199..74794744hg38UCSC Ensembl
chr15:75083561..75087064hg19UCSC Ensembl
Innerchr15:75083582..75087043hg19UCSC Ensembl
Outerchr15:75083540..75087085hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383504
hg193504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292831, essv15292830
SamplesNA18745, HG00728
Known GenesCSK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636909
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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