A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3382751



Internal ID15229722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90098550..90099748hg38UCSC Ensembl
Innerchr9:90098748..90099550hg38UCSC Ensembl
Outerchr9:90097550..90100748hg38UCSC Ensembl
chr9:92860832..92862030hg19UCSC Ensembl
Innerchr9:92861030..92861832hg19UCSC Ensembl
Outerchr9:92859832..92863030hg19UCSC Ensembl
chr9:91900652..91901850hg18UCSC Ensembl
Innerchr9:91901652..91900850hg18UCSC Ensembl
Outerchr9:91899652..91902850hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697417
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3382751
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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