A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3394258



Internal ID15241223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1850715..1850734hg38UCSC Ensembl
Innerchr9:1850711..1850738hg38UCSC Ensembl
Outerchr9:1850692..1850757hg38UCSC Ensembl
chr9:1850715..1850734hg19UCSC Ensembl
Innerchr9:1850711..1850738hg19UCSC Ensembl
Outerchr9:1850692..1850757hg19UCSC Ensembl
chr9:1840715..1840734hg18UCSC Ensembl
Innerchr9:1840738..1840711hg18UCSC Ensembl
Outerchr9:1840692..1840757hg18UCSC Ensembl
Cytoband9p24.3
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 Variantsessv9642115
SamplesNA19143
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3394258
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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