A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583455



Internal ID21531980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150062175..150062599hg38UCSC Ensembl
chr5:149441738..149442162hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124601
SamplesHG00512
Known GenesCSF1R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583455
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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