A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621176



Internal ID7008045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96932909..96985176hg38UCSC Ensembl
Innerchr9:96933409..96984676hg38UCSC Ensembl
Outerchr9:96931909..96986176hg38UCSC Ensembl
chr9:99695191..99747458hg19UCSC Ensembl
Innerchr9:99695691..99746958hg19UCSC Ensembl
Outerchr9:99694191..99748458hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3852268
hg1952268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13573479
SamplesHG00458
Known GenesHIATL2, NUTM2G
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621176
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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