A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13459385



Internal ID3461201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35504377..35568617hg38UCSC Ensembl
chr9:35504374..35568614hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3864241
hg1964241
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620379
Supporting Variants
SamplesHG00674
Known GenesFAM166B, RUSC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13459385
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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