A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841169



Internal ID22616104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:144175848..144180890hg38UCSC Ensembl
chr5:143555411..143560453hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg385043
hg195043
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496207
Samples
Known GenesKCTD16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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