A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3411421



Internal ID14911695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64026100..64026124hg38UCSC Ensembl
Innerchr1:64026110..64026112hg38UCSC Ensembl
Outerchr1:64026086..64026136hg38UCSC Ensembl
chr1:64491772..64491796hg19UCSC Ensembl
Innerchr1:64491782..64491784hg19UCSC Ensembl
Outerchr1:64491758..64491808hg19UCSC Ensembl
chr1:64264360..64264384hg18UCSC Ensembl
Innerchr1:64264372..64264370hg18UCSC Ensembl
Outerchr1:64264346..64264396hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38257
hg19257
hg18257
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8674056
SamplesNA19238
Known GenesROR1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3411421
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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