A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8670709



Internal ID13308617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33058003..33058086hg38UCSC Ensembl
Innerchr15:33058033..33058054hg38UCSC Ensembl
Outerchr15:33057971..33058116hg38UCSC Ensembl
chr15:33350204..33350287hg19UCSC Ensembl
Innerchr15:33350234..33350255hg19UCSC Ensembl
Outerchr15:33350172..33350317hg19UCSC Ensembl
chr15:31137496..31137579hg18UCSC Ensembl
Innerchr15:31137526..31137547hg18UCSC Ensembl
Outerchr15:31137464..31137609hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3884
hg1984
hg1884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3385230
Supporting Variants
SamplesNA12878
Known GenesFMN1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8670709
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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