A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636230



Internal ID6676339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40725701..40726625hg38UCSC Ensembl
Innerchr15:40725751..40726575hg38UCSC Ensembl
Outerchr15:40725597..40726729hg38UCSC Ensembl
chr15:41017899..41018823hg19UCSC Ensembl
Innerchr15:41017949..41018773hg19UCSC Ensembl
Outerchr15:41017795..41018927hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15228207
SamplesHG01990
Known GenesRAD51
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636230
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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