A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7743961



Internal ID13855380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34063161..34063162hg38UCSC Ensembl
Innerchr13:34063126..34063197hg38UCSC Ensembl
Outerchr13:34063125..34063198hg38UCSC Ensembl
chr13:34637298..34637299hg19UCSC Ensembl
Innerchr13:34637263..34637334hg19UCSC Ensembl
Outerchr13:34637262..34637335hg19UCSC Ensembl
chr13:33535298..33535299hg18UCSC Ensembl
Innerchr13:33535334..33535263hg18UCSC Ensembl
Outerchr13:33535262..33535335hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38295
hg19295
hg18295
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305858
Supporting Variants
SamplesNA18511
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7743961
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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