A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13622641



Internal ID3624457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127863894..127881499hg38UCSC Ensembl
chr9:130626173..130643778hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3817606
hg1917606
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621795
Supporting Variants
SamplesNA12414
Known GenesAK1, MIR4672
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13622641
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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