A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419519



Internal ID22477389
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 StatusS
Merged Variantsnsv5905704
Supporting Variants
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419519
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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