A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13641434



Internal ID1183461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134245815..134270075hg38UCSC Ensembl
chr9:137137661..137161921hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3824261
hg1924261
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621957
Supporting Variants
SamplesHG01061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13641434
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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