A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489331



Internal ID22547250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220832471..220836178hg38UCSC Ensembl
chr2:221697191..221700898hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg383708
hg193708
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489331
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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