A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471498



Internal ID22529389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4635448..4636947hg38UCSC Ensembl
chr16:4685449..4686948hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870219
Supporting Variants
Samples
Known GenesMGRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471498
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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