A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809569



Internal ID13652883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137102059..137102744hg38UCSC Ensembl
Innerchr9:137102058..137102745hg38UCSC Ensembl
Outerchr9:137101949..137102864hg38UCSC Ensembl
chr9:139996511..139997196hg19UCSC Ensembl
Innerchr9:139996510..139997197hg19UCSC Ensembl
Outerchr9:139996401..139997316hg19UCSC Ensembl
chr9:139116332..139117017hg18UCSC Ensembl
Innerchr9:139117018..139116331hg18UCSC Ensembl
Outerchr9:139116222..139117137hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38686
hg19686
hg18686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3376450
Supporting Variants
SamplesNA12878
Known GenesMAN1B1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809569
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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