A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492609



Internal ID22550537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47937787..47941220hg38UCSC Ensembl
chr3:47979277..47982710hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383434
hg193434
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836346
Supporting Variants
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492609
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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