A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906881



Internal ID22682085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64705357..64705511hg38UCSC Ensembl
chr5:64001184..64001338hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416498
Samples
Known GenesFAM159B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906881
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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