A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8951009



Internal ID14211673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128826789..128826803hg38UCSC Ensembl
Innerchr10:128826787..128826803hg38UCSC Ensembl
Outerchr10:128826773..128826817hg38UCSC Ensembl
chr10:130625053..130625067hg19UCSC Ensembl
Innerchr10:130625051..130625067hg19UCSC Ensembl
Outerchr10:130625037..130625081hg19UCSC Ensembl
chr10:130515043..130515057hg18UCSC Ensembl
Innerchr10:130515057..130515041hg18UCSC Ensembl
Outerchr10:130515027..130515071hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386009
hg196009
hg186009
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3406205
Supporting Variants
SamplesNA18577
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8951009
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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