A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698094



Internal ID21219944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084376..150084470hg38UCSC Ensembl
chr5:149463939..149464033hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810556
Supporting Variants
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698094
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.375


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