A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492190



Internal ID22550117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9597543..9601993hg38UCSC Ensembl
chr3:9639227..9643677hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384451
hg194451
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837248
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492190
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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