A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3406931



Internal ID15253893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68775573..68775573hg38UCSC Ensembl
Innerchr10:68775572..68775574hg38UCSC Ensembl
Outerchr10:68775523..68775623hg38UCSC Ensembl
chr10:70535330..70535330hg19UCSC Ensembl
Innerchr10:70535329..70535331hg19UCSC Ensembl
Outerchr10:70535280..70535380hg19UCSC Ensembl
chr10:70205336..70205336hg18UCSC Ensembl
Innerchr10:70205337..70205335hg18UCSC Ensembl
Outerchr10:70205286..70205386hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38403
hg19403
hg18403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8740702
SamplesNA19240
Known GenesCCAR1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3406931
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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