A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651925



Internal ID15100576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74216501..74216728hg38UCSC Ensembl
Innerchr15:74216501..74216728hg38UCSC Ensembl
Outerchr15:74215659..74217636hg38UCSC Ensembl
chr15:74508842..74509069hg19UCSC Ensembl
Innerchr15:74508842..74509069hg19UCSC Ensembl
Outerchr15:74508000..74509977hg19UCSC Ensembl
chr15:72295895..72296122hg18UCSC Ensembl
Innerchr15:72295895..72296122hg18UCSC Ensembl
Outerchr15:72295053..72297030hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38228
hg19228
hg18228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3351294
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651925
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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