A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485729



Internal ID22543641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153476968..153489222hg38UCSC Ensembl
chr3:153194757..153207011hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3812255
hg1912255
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835001
Supporting Variants
Samples
Known GenesC3orf79
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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