A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13570836



Internal ID3572652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94624578..94629601hg38UCSC Ensembl
Innerchr9:94624628..94629551hg38UCSC Ensembl
Outerchr9:94624462..94629717hg38UCSC Ensembl
chr9:97386860..97391883hg19UCSC Ensembl
Innerchr9:97386910..97391833hg19UCSC Ensembl
Outerchr9:97386744..97391999hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385024
hg195024
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621134
Supporting Variants
SamplesNA20775
Known GenesFBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13570836
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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