A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13573597



Internal ID4143117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97142021..97167142hg38UCSC Ensembl
Innerchr9:97142021..97167142hg38UCSC Ensembl
Outerchr9:97141521..97167642hg38UCSC Ensembl
chr9:99904303..99929424hg19UCSC Ensembl
Innerchr9:99904303..99929424hg19UCSC Ensembl
Outerchr9:99903803..99929924hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3825122
hg1925122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621183
Supporting Variants
SamplesHG03752
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13573597
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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