A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697405



Internal ID15028599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88973117..88974815hg38UCSC Ensembl
Innerchr9:88973815..88974117hg38UCSC Ensembl
Outerchr9:88972117..88975815hg38UCSC Ensembl
chr9:91588032..91589730hg19UCSC Ensembl
Innerchr9:91588730..91589032hg19UCSC Ensembl
Outerchr9:91587032..91590730hg19UCSC Ensembl
chr9:90777852..90779550hg18UCSC Ensembl
Innerchr9:90778852..90778550hg18UCSC Ensembl
Outerchr9:90776852..90780550hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3375962
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697405
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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