A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483122



Internal ID22541029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102769323..102776693hg38UCSC Ensembl
chr3:102488167..102495537hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg387371
hg197371
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483122
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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