A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487088



Internal ID22545003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16743240..16755781hg38UCSC Ensembl
chr3:16784747..16797288hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3812542
hg1912542
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487088
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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