A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491629



Internal ID22549555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35240625..35268604hg38UCSC Ensembl
chr3:35282117..35310096hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3827980
hg1927980
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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