A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677483



Internal ID15025085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91510801..91510820hg38UCSC Ensembl
Innerchr9:91510806..91510815hg38UCSC Ensembl
Outerchr9:91510787..91510834hg38UCSC Ensembl
chr9:94273083..94273102hg19UCSC Ensembl
Innerchr9:94273088..94273097hg19UCSC Ensembl
Outerchr9:94273069..94273116hg19UCSC Ensembl
chr9:93312904..93312923hg18UCSC Ensembl
Innerchr9:93312918..93312909hg18UCSC Ensembl
Outerchr9:93312890..93312937hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38268
hg19268
hg18268
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3347069
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677483
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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