A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13572581



Internal ID4748213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96137580..96151027hg38UCSC Ensembl
chr9:98899862..98913309hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3813448
hg1913448
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621160
Supporting Variants
SamplesNA07347
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13572581
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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