A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620510



Internal ID7007381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43005069..43033698hg38UCSC Ensembl
chr9:66284867..66313496hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3828630
hg1928630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13493900, essv13493897, essv13493899, essv13493896, essv13493901, essv13493898, essv13493895
SamplesHG01412, HG04229, HG03667, HG03736, NA18630, NA18615, HG03922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620510
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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