A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8679432



Internal ID15109964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35148174..35148193hg38UCSC Ensembl
Innerchr9:35148170..35148197hg38UCSC Ensembl
Outerchr9:35148151..35148216hg38UCSC Ensembl
chr9:35148171..35148190hg19UCSC Ensembl
Innerchr9:35148167..35148194hg19UCSC Ensembl
Outerchr9:35148148..35148213hg19UCSC Ensembl
chr9:35138171..35138190hg18UCSC Ensembl
Innerchr9:35138194..35138167hg18UCSC Ensembl
Outerchr9:35138148..35138213hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3432107
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8679432
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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