A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453055



Internal ID21110608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111008201..111016500hg38UCSC Ensembl
chr9:113770481..113778780hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174554
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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