A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489713



Internal ID22547633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177549795..177552869hg38UCSC Ensembl
chr3:177267583..177270657hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383075
hg193075
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835681
Supporting Variants
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489713
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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