A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490417



Internal ID22548340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194171052..194174754hg38UCSC Ensembl
chr3:193888841..193892543hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg383703
hg193703
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490417
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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