A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909063



Internal ID22684273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97776107..97805350hg38UCSC Ensembl
chr8:98788335..98817578hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3829244
hg1929244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437757
Samples
Known GenesLAPTM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909063
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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