A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482058



Internal ID22539963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210977323..210985790hg38UCSC Ensembl
chr2:211842047..211850514hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg388468
hg198468
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482058
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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