A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3366188



Internal ID15213165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68230416..68236414hg38UCSC Ensembl
Innerchr9:68231416..68235414hg38UCSC Ensembl
Outerchr9:68229416..68237414hg38UCSC Ensembl
chr9:70845332..70851330hg19UCSC Ensembl
Innerchr9:70846332..70850330hg19UCSC Ensembl
Outerchr9:70844332..70852330hg19UCSC Ensembl
chr9:70035152..70041150hg18UCSC Ensembl
Innerchr9:70036152..70040150hg18UCSC Ensembl
Outerchr9:70034152..70042150hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg385999
hg195999
hg185999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697370
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3366188
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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