A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3383319



Internal ID15230290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38047034..38047051hg38UCSC Ensembl
Innerchr15:38047035..38047050hg38UCSC Ensembl
Outerchr15:38047018..38047067hg38UCSC Ensembl
chr15:38339235..38339252hg19UCSC Ensembl
Innerchr15:38339236..38339251hg19UCSC Ensembl
Outerchr15:38339219..38339268hg19UCSC Ensembl
chr15:36126527..36126544hg18UCSC Ensembl
Innerchr15:36126543..36126528hg18UCSC Ensembl
Outerchr15:36126511..36126560hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38211
hg19211
hg18211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8673157
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3383319
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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