A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492626



Internal ID22550554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48344586..48353385hg38UCSC Ensembl
chr3:48386076..48394875hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492626
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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