A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488681



Internal ID22546598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94239415..94241575hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382161
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488681
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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