A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663539



Internal ID9929644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89040497..89053020hg38UCSC Ensembl
Outerchr15:89040325..89053205hg38UCSC Ensembl
Innerchr15:89583728..89596251hg19UCSC Ensembl
Outerchr15:89583556..89596436hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812881
hg1912881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6020327, essv6482414
SamplesHG00428, NA18624
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663539
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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