A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9649524



Internal ID13368656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110003190..110003209hg38UCSC Ensembl
Innerchr10:110003186..110003213hg38UCSC Ensembl
Outerchr10:110003167..110003232hg38UCSC Ensembl
chr10:111762948..111762967hg19UCSC Ensembl
Innerchr10:111762944..111762971hg19UCSC Ensembl
Outerchr10:111762925..111762990hg19UCSC Ensembl
chr10:111752938..111752957hg18UCSC Ensembl
Innerchr10:111752961..111752934hg18UCSC Ensembl
Outerchr10:111752915..111752980hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3448340
Supporting Variants
SamplesNA12045
Known GenesADD3-AS1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9649524
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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