A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484900



Internal ID22542810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:103789435..103793915hg38UCSC Ensembl
chr2:104405893..104410373hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg384481
hg194481
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830565
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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