A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13595270



Internal ID3597086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109143603..109144777hg38UCSC Ensembl
Innerchr9:109143638..109144742hg38UCSC Ensembl
Outerchr9:109143568..109144812hg38UCSC Ensembl
chr9:111905883..111907057hg19UCSC Ensembl
Innerchr9:111905918..111907022hg19UCSC Ensembl
Outerchr9:111905848..111907092hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621430
Supporting Variants
SamplesNA19332
Known GenesFRRS1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13595270
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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