A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894657



Internal ID22669731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122782606..122783005hg38UCSC Ensembl
chr5:122118301..122118700hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428871
Samples
Known GenesSNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894657
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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