A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902849



Internal ID22678011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173608292..173609236hg38UCSC Ensembl
chr5:173035295..173036239hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410518
Samples
Known GenesBOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902849
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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