A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13657437



Internal ID4592787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136971978..136976727hg38UCSC Ensembl
chr9:139866430..139871179hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384750
hg194750
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622018
Supporting Variants
SamplesHG04106
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13657437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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