A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486466



Internal ID22544380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156585770..156590298hg38UCSC Ensembl
chr3:156303559..156308087hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384529
hg194529
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835045
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486466
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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