A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669137



Internal ID9935242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37850099..37851192hg38UCSC Ensembl
Outerchr15:37849942..37851345hg38UCSC Ensembl
Innerchr15:38142300..38143393hg19UCSC Ensembl
Outerchr15:38142143..38143546hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6517800, essv5882006
SamplesHG00189, HG00325
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669137
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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