A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8944330



Internal ID14839875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30989611..30989641hg38UCSC Ensembl
Innerchr9:30989623..30989627hg38UCSC Ensembl
Outerchr9:30989595..30989657hg38UCSC Ensembl
chr9:30989609..30989639hg19UCSC Ensembl
Innerchr9:30989621..30989625hg19UCSC Ensembl
Outerchr9:30989593..30989655hg19UCSC Ensembl
chr9:30979609..30979639hg18UCSC Ensembl
Innerchr9:30979625..30979621hg18UCSC Ensembl
Outerchr9:30979593..30979655hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3375636
Supporting Variants
SamplesNA19102
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8944330
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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