A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416128



Internal ID22473998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86348131..86353801hg38UCSC Ensembl
chr5:85643949..85649619hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385671
hg195671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416128
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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