A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3304829



Internal ID15151777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129446220..129446221hg38UCSC Ensembl
Innerchr10:129446198..129446243hg38UCSC Ensembl
Outerchr10:129446197..129446244hg38UCSC Ensembl
chr10:131244484..131244485hg19UCSC Ensembl
Innerchr10:131244462..131244507hg19UCSC Ensembl
Outerchr10:131244461..131244508hg19UCSC Ensembl
chr10:131134474..131134475hg18UCSC Ensembl
Innerchr10:131134497..131134452hg18UCSC Ensembl
Outerchr10:131134451..131134498hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38269
hg19269
hg18269
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7766536
SamplesNA12814
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3304829
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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