A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3451136



Internal ID14951397
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 StatusM
Merged Variants
Supporting Variantsessv8697390
SamplesNA19239
Known GenesKIF27
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3451136
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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