A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13639277



Internal ID3641093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133252403..133258233hg38UCSC Ensembl
Innerchr9:133252404..133258233hg38UCSC Ensembl
Outerchr9:133252403..133258234hg38UCSC Ensembl
chr9:136127790..136133624hg19UCSC Ensembl
Innerchr9:136127791..136133624hg19UCSC Ensembl
Outerchr9:136127790..136133625hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385831
hg195835
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621936
Supporting Variants
SamplesHG03559
Known GenesABO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13639277
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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