A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908095



Internal ID22683305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102234648..102235360hg38UCSC Ensembl
chr8:103246876..103247588hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436888
Samples
Known GenesRRM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908095
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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