A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888167



Internal ID22663168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145689921..145690221hg38UCSC Ensembl
chr4:146611073..146611373hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410020
Samples
Known GenesC4orf51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888167
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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