A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505902



Internal ID22563846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50476641..50479598hg38UCSC Ensembl
chr6:50444354..50447311hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382958
hg192958
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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