A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9644114



Internal ID13604952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87276750..87276769hg38UCSC Ensembl
Innerchr9:87276746..87276773hg38UCSC Ensembl
Outerchr9:87276727..87276792hg38UCSC Ensembl
chr9:89891665..89891684hg19UCSC Ensembl
Innerchr9:89891661..89891688hg19UCSC Ensembl
Outerchr9:89891642..89891707hg19UCSC Ensembl
chr9:89081485..89081504hg18UCSC Ensembl
Innerchr9:89081508..89081481hg18UCSC Ensembl
Outerchr9:89081462..89081527hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3332946
Supporting Variants
SamplesNA12814
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9644114
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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