A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736456



Internal ID20512405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084348..150084451hg38UCSC Ensembl
chr5:149463911..149464014hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296549
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736456
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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