A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7732919



Internal ID14096883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70776194..70776405hg38UCSC Ensembl
Outerchr10:70775994..70776605hg38UCSC Ensembl
Innerchr10:72535950..72536161hg19UCSC Ensembl
Outerchr10:72535750..72536361hg19UCSC Ensembl
Innerchr10:72205956..72206167hg18UCSC Ensembl
Outerchr10:72205756..72206367hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38612
hg19612
hg18612
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302857
Supporting Variants
SamplesNA18563
Known GenesTBATA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7732919
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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