A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3354144



Internal ID14854408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121777461..121777480hg38UCSC Ensembl
Innerchr10:121777457..121777484hg38UCSC Ensembl
Outerchr10:121777438..121777503hg38UCSC Ensembl
chr10:123536976..123536995hg19UCSC Ensembl
Innerchr10:123536972..123536999hg19UCSC Ensembl
Outerchr10:123536953..123537018hg19UCSC Ensembl
chr10:123526966..123526985hg18UCSC Ensembl
Innerchr10:123526989..123526962hg18UCSC Ensembl
Outerchr10:123526943..123527008hg18UCSC Ensembl
Cytoband10q26.13
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 Variantsessv9649892
SamplesNA19143
Known GenesATE1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3354144
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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