A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3392785



Internal ID15239750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171908574..171908593hg38UCSC Ensembl
Innerchr3:171908570..171908597hg38UCSC Ensembl
Outerchr3:171908551..171908616hg38UCSC Ensembl
chr3:171626364..171626383hg19UCSC Ensembl
Innerchr3:171626360..171626387hg19UCSC Ensembl
Outerchr3:171626341..171626406hg19UCSC Ensembl
chr3:173109058..173109077hg18UCSC Ensembl
Innerchr3:173109081..173109054hg18UCSC Ensembl
Outerchr3:173109035..173109100hg18UCSC Ensembl
Cytoband3q26.31
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 Variantsessv9613157, essv9613179, essv9613190, essv9613168
SamplesNA07347, NA12249, NA12043, NA11881
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3392785
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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