A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489670



Internal ID22547590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175302024..175312251hg38UCSC Ensembl
chr3:175019813..175030040hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810228
hg1910228
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835126
Supporting Variants
Samples
Known GenesNAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489670
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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