A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8947263



Internal ID14216431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17709963..17709974hg38UCSC Ensembl
Innerchr10:17709953..17709981hg38UCSC Ensembl
Outerchr10:17709942..17709992hg38UCSC Ensembl
chr10:17751962..17751973hg19UCSC Ensembl
Innerchr10:17751952..17751980hg19UCSC Ensembl
Outerchr10:17751941..17751991hg19UCSC Ensembl
chr10:17791968..17791979hg18UCSC Ensembl
Innerchr10:17791986..17791958hg18UCSC Ensembl
Outerchr10:17791947..17791997hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3406363
Supporting Variants
SamplesNA18577
Known GenesSTAM
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8947263
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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