A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174546



Internal ID20741586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110962312..110962952hg38UCSC Ensembl
chr9:113724592..113725232hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451147
Supporting Variants
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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