A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414049



Internal ID22471919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16093033..16093090hg38UCSC Ensembl
chr5:16093142..16093199hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904616
Supporting Variants
Samples
Known GenesMARCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414049
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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