A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495436



Internal ID22553369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78586131..78587320hg38UCSC Ensembl
chr3:78635281..78636470hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837057
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495436
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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