A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411242



Internal ID22469112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10246265..10247914hg38UCSC Ensembl
chr5:10246377..10248026hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889302
Supporting Variants
Samples
Known GenesFAM173B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411242
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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