A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133303



Internal ID21416022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084364..150084466hg38UCSC Ensembl
chr5:149463927..149464029hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572493
Supporting Variants
SamplesHG00731
Known GenesCSF1R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133303
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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