A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3324317



Internal ID15171295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34323325..34323363hg38UCSC Ensembl
Innerchr10:34323331..34323355hg38UCSC Ensembl
Outerchr10:34323295..34323393hg38UCSC Ensembl
chr10:34612253..34612291hg19UCSC Ensembl
Innerchr10:34612259..34612283hg19UCSC Ensembl
Outerchr10:34612223..34612321hg19UCSC Ensembl
chr10:34652259..34652297hg18UCSC Ensembl
Innerchr10:34652289..34652265hg18UCSC Ensembl
Outerchr10:34652229..34652327hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38213
hg19213
hg18213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8671791
SamplesNA19238
Known GenesPARD3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3324317
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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