A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661332



Internal ID9927437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81385393..81385537hg38UCSC Ensembl
Outerchr15:81385236..81385690hg38UCSC Ensembl
Innerchr15:81677734..81677878hg19UCSC Ensembl
Outerchr15:81677577..81678031hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5797383, essv5450899, essv5860678, essv6296407, essv5800591, essv6209062, essv6139914, essv5766895, essv5710934, essv6012453, essv5552035, essv6487218, essv5691590, essv6106862, essv5565102, essv5425081
SamplesHG01462, HG00142, HG01374, NA12399, HG01070, HG00122, HG00346, HG01365, NA20539, HG01519, HG00133, HG00275, NA20785, NA19759, HG00342, HG01516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661332
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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