A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13628962



Internal ID3106768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129892709..130036621hg38UCSC Ensembl
chr9:132654988..132798900hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38143913
hg19143913
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621845
Supporting Variants
SamplesHG02727
Known GenesFNBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13628962
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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