A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8967903



Internal ID14389169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38047058..38047078hg38UCSC Ensembl
Innerchr15:38047057..38047076hg38UCSC Ensembl
Outerchr15:38047040..38047096hg38UCSC Ensembl
chr15:38339259..38339279hg19UCSC Ensembl
Innerchr15:38339258..38339277hg19UCSC Ensembl
Outerchr15:38339241..38339297hg19UCSC Ensembl
chr15:36126551..36126571hg18UCSC Ensembl
Innerchr15:36126569..36126550hg18UCSC Ensembl
Outerchr15:36126533..36126589hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38217
hg19217
hg18217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3328613
Supporting Variants
SamplesNA18870
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8967903
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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