A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482049



Internal ID22539954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209306406..209311358hg38UCSC Ensembl
chr2:210171130..210176082hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg384953
hg194953
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482049
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer