A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480690



Internal ID22538594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175181967..175199931hg38UCSC Ensembl
chr2:176046695..176064659hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3817965
hg1917965
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480690
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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