A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303546



Internal ID14803808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77236403..77236404hg38UCSC Ensembl
Innerchr10:77236381..77236426hg38UCSC Ensembl
Outerchr10:77236380..77236427hg38UCSC Ensembl
chr10:78996161..78996162hg19UCSC Ensembl
Innerchr10:78996139..78996184hg19UCSC Ensembl
Outerchr10:78996138..78996185hg19UCSC Ensembl
chr10:78666167..78666168hg18UCSC Ensembl
Innerchr10:78666190..78666145hg18UCSC Ensembl
Outerchr10:78666144..78666191hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38169
hg19169
hg18169
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7768502
SamplesNA12872
Known GenesKCNMA1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303546
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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