A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636229



Internal ID6676338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40719322..40727579hg38UCSC Ensembl
Innerchr15:40719472..40727429hg38UCSC Ensembl
Outerchr15:40719172..40727729hg38UCSC Ensembl
chr15:41011520..41019777hg19UCSC Ensembl
Innerchr15:41011670..41019627hg19UCSC Ensembl
Outerchr15:41011370..41019927hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg388258
hg198258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15228206
SamplesHG02537
Known GenesRAD51
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636229
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer