A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13601047



Internal ID3602863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110896895..110926031hg38UCSC Ensembl
Innerchr9:110896977..110925949hg38UCSC Ensembl
Outerchr9:110896813..110926113hg38UCSC Ensembl
chr9:113659175..113688311hg19UCSC Ensembl
Innerchr9:113659257..113688229hg19UCSC Ensembl
Outerchr9:113659093..113688393hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3829137
hg1929137
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621475
Supporting Variants
SamplesHG00533
Known GenesLPAR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13601047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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