A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3421920



Internal ID15268878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119848166..119848181hg38UCSC Ensembl
Innerchr10:119848140..119848207hg38UCSC Ensembl
Outerchr10:119848125..119848222hg38UCSC Ensembl
chr10:121607678..121607693hg19UCSC Ensembl
Innerchr10:121607652..121607719hg19UCSC Ensembl
Outerchr10:121607637..121607734hg19UCSC Ensembl
chr10:121597668..121597683hg18UCSC Ensembl
Innerchr10:121597709..121597642hg18UCSC Ensembl
Outerchr10:121597627..121597724hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865417
SamplesNA12005
Known GenesMCMBP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3421920
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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