A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688093



Internal ID13371277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46402604..46415905hg38UCSC Ensembl
Innerchr10:46403604..46414903hg38UCSC Ensembl
Outerchr10:46401619..46416909hg38UCSC Ensembl
chr10:47133846..47147144hg19UCSC Ensembl
Innerchr10:47134846..47146144hg19UCSC Ensembl
Outerchr10:47132846..47148144hg19UCSC Ensembl
chr10:46553852..46567150hg18UCSC Ensembl
Innerchr10:46554852..46566150hg18UCSC Ensembl
Outerchr10:46552852..46568150hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3813302
hg1913299
hg1813299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3391435
Supporting Variants
SamplesNA12892
Known GenesLINC00842
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688093
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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