A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697390



Internal ID14715196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83900117..83901615hg38UCSC Ensembl
Innerchr9:83900615..83901117hg38UCSC Ensembl
Outerchr9:83899117..83902615hg38UCSC Ensembl
chr9:86515032..86516530hg19UCSC Ensembl
Innerchr9:86515530..86516032hg19UCSC Ensembl
Outerchr9:86514032..86517530hg19UCSC Ensembl
chr9:85704852..85706350hg18UCSC Ensembl
Innerchr9:85705852..85705350hg18UCSC Ensembl
Outerchr9:85703852..85707350hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3451136
Supporting Variants
SamplesNA19239
Known GenesKIF27
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697390
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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