A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502943



Internal ID22560884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16258994..16264506hg38UCSC Ensembl
chr6:16259225..16264737hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385513
hg195513
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844448
Supporting Variants
Samples
Known GenesGMPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502943
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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