A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13491714



Internal ID426346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61660998..61699030hg38UCSC Ensembl
chr9:44868836..44906868hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3838033
hg1938033
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620499
Supporting Variants
SamplesHG00129
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13491714
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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