A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620486



Internal ID7007357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42730139..42763058hg38UCSC Ensembl
chr9:44208061..44240980hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3832920
hg1932920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13482486, essv13482479, essv13482484, essv13482480, essv13482485, essv13482481, essv13482487, essv13482483, essv13482482, essv13482478
SamplesHG04229, HG03667, HG01997, HG03736, NA20355, HG02879, NA19747, NA18615, NA20334, HG03922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620486
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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