A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488308



Internal ID22546225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164353690..164354741hg38UCSC Ensembl
chr2:165210200..165211251hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488308
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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