A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567363



Internal ID21759406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084387..150084387hg38UCSC Ensembl
chr5:149463950..149463950hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063168
Supporting Variants
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567363
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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