A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620482



Internal ID7007353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42830430..42870611hg38UCSC Ensembl
chr9:44100508..44140689hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3840182
hg1940182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13482434, essv13482430, essv13482432, essv13482433, essv13482436, essv13482437, essv13482435, essv13482431
SamplesHG04229, HG03667, HG03736, HG01088, NA18630, NA18615, HG02079, HG03922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620482
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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