A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688094



Internal ID13286036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46400219..46415805hg38UCSC Ensembl
Innerchr10:46401219..46414803hg38UCSC Ensembl
Outerchr10:46399219..46416809hg38UCSC Ensembl
chr10:47133946..47149544hg19UCSC Ensembl
Innerchr10:47134946..47148544hg19UCSC Ensembl
Outerchr10:47132946..47150544hg19UCSC Ensembl
chr10:46553952..46569550hg18UCSC Ensembl
Innerchr10:46554952..46568550hg18UCSC Ensembl
Outerchr10:46552952..46570550hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3815587
hg1915599
hg1815599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3413028
Supporting Variants
SamplesNA12878
Known GenesLINC00842
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688094
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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