A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488345



Internal ID22546262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16593854..16596254hg38UCSC Ensembl
chr21:17966174..17968574hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382401
hg192401
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879871
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488345
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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