A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697429



Internal ID15062265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92803749..92805347hg38UCSC Ensembl
Innerchr9:92804347..92804749hg38UCSC Ensembl
Outerchr9:92802749..92806347hg38UCSC Ensembl
chr9:95566031..95567629hg19UCSC Ensembl
Innerchr9:95566629..95567031hg19UCSC Ensembl
Outerchr9:95565031..95568629hg19UCSC Ensembl
chr9:94605852..94607450hg18UCSC Ensembl
Innerchr9:94606852..94606450hg18UCSC Ensembl
Outerchr9:94604852..94608450hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3394460
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697429
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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