A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15228206



Internal ID2863084
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636229
Supporting Variants
SamplesHG02537
Known GenesRAD51
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15228206
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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