A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3344326



Internal ID14844593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28857369..28857388hg38UCSC Ensembl
Innerchr10:28857365..28857392hg38UCSC Ensembl
Outerchr10:28857346..28857411hg38UCSC Ensembl
chr10:29146298..29146317hg19UCSC Ensembl
Innerchr10:29146294..29146321hg19UCSC Ensembl
Outerchr10:29146275..29146340hg19UCSC Ensembl
chr10:29186304..29186323hg18UCSC Ensembl
Innerchr10:29186327..29186300hg18UCSC Ensembl
Outerchr10:29186281..29186346hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9646769, essv9646747, essv9646758
SamplesNA12815, NA19143, NA18970
Known GenesC10orf126
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3344326
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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