A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3435683



Internal ID15282637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62445155..62453053hg38UCSC Ensembl
Innerchr9:62446155..62452053hg38UCSC Ensembl
Outerchr9:62444155..62454053hg38UCSC Ensembl
chr9:46756456..46764354hg19UCSC Ensembl
Innerchr9:46757456..46763354hg19UCSC Ensembl
Outerchr9:46755456..46765354hg19UCSC Ensembl
chr9:46596452..46604350hg18UCSC Ensembl
Innerchr9:46597452..46603350hg18UCSC Ensembl
Outerchr9:46595452..46605350hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg387899
hg197899
hg187899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4375e59
Supporting Variantsessv8696980
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3435683
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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