A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696966



Internal ID13732216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62357755..62365753hg38UCSC Ensembl
Innerchr9:62358755..62364753hg38UCSC Ensembl
Outerchr9:62356755..62366753hg38UCSC Ensembl
chr9:46669056..46677054hg19UCSC Ensembl
Innerchr9:46670056..46676054hg19UCSC Ensembl
Outerchr9:46668056..46678054hg19UCSC Ensembl
chr9:46509052..46517050hg18UCSC Ensembl
Innerchr9:46510052..46516050hg18UCSC Ensembl
Outerchr9:46508052..46518050hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg387999
hg197999
hg187999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3367554
Supporting Variants
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696966
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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