A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13569263



Internal ID5553031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94279979..94482067hg38UCSC Ensembl
chr9:97042261..97244349hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38202089
hg19202089
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621117
Supporting Variants
SamplesNA19006
Known GenesHIATL1, LOC100132077, NUTM2F, ZNF169
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13569263
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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