A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490657



Internal ID22548581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30936092..30950639hg38UCSC Ensembl
chr3:30977584..30992131hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3814548
hg1914548
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490657
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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