A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13383152



Internal ID4424727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4416209..4446921hg38UCSC Ensembl
Innerchr9:4416226..4446905hg38UCSC Ensembl
Outerchr9:4416193..4446938hg38UCSC Ensembl
chr9:4416209..4446921hg19UCSC Ensembl
Innerchr9:4416226..4446905hg19UCSC Ensembl
Outerchr9:4416193..4446938hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3830713
hg1930713
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619341
Supporting Variants
SamplesHG03940
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13383152
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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