A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13606606



Internal ID3608422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113090158..113120352hg38UCSC Ensembl
chr9:115852438..115882632hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3830195
hg1930195
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621529
Supporting Variants
SamplesHG02941
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13606606
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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