A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15228046



Internal ID5229862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40529692..40531361hg38UCSC Ensembl
Innerchr15:40529703..40531350hg38UCSC Ensembl
Outerchr15:40529681..40531372hg38UCSC Ensembl
chr15:40821891..40823560hg19UCSC Ensembl
Innerchr15:40821902..40823549hg19UCSC Ensembl
Outerchr15:40821880..40823571hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381670
hg191670
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636227
Supporting Variants
SamplesHG02774
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15228046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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